import pytest


@pytest.fixture
def associations():
    return {
        "limit": 20,
        "offset": 0,
        "total": 11903,
        "items": [
            {
                "id": "uuid:11cb9475-198e-11f0-be82-6045bdb3d4c0",
                "category": "biolink:GeneToPhenotypicFeatureAssociation",
                "subject": "HGNC:27337",
                "original_subject": "NCBIGene:203859",
                "subject_namespace": "HGNC",
                "subject_category": "biolink:Gene",
                "subject_closure": None,
                "subject_label": "ANO5",
                "subject_closure_label": None,
                "subject_taxon": "NCBITaxon:9606",
                "subject_taxon_label": "Homo sapiens",
                "predicate": "biolink:has_phenotype",
                "original_predicate": None,
                "object": "HP:0001371",
                "original_object": None,
                "object_namespace": "HP",
                "object_category": "biolink:PhenotypicFeature",
                "object_closure": [
                    "HP:0001371",
                    "UPHENO:0046638",
                    "UPHENO:0069327",
                    "UPHENO:0069218",
                    "UPHENO:0002949",
                    "UPHENO:0068971",
                    "UPHENO:0003047",
                    "UPHENO:0002712",
                    "UBERON:0000062",
                    "UBERON:0000468",
                    "UPHENO:0082875",
                    "UPHENO:0069266",
                    "UPHENO:0046483",
                    "UPHENO:0046606",
                    "UBERON:0004770",
                    "UBERON:0002384",
                    "HP:0011842",
                    "HP:0011805",
                    "UPHENO:0081581",
                    "UPHENO:0002568",
                    "UPHENO:0046552",
                    "UPHENO:0046505",
                    "HP:0000924",
                    "HP:0003011",
                    "UPHENO:0003432",
                    "UPHENO:0002526",
                    "UPHENO:0076703",
                    "HP:0000118",
                    "BFO:0000004",
                    "UPHENO:0002564",
                    "UPHENO:0002976",
                    "UBERON:0001062",
                    "UBERON:0000061",
                    "UBERON:0005090",
                    "UPHENO:0002269",
                    "UPHENO:0001002",
                    "UPHENO:0075195",
                    "HP:0033127",
                    "UPHENO:0001003",
                    "UPHENO:0088186",
                    "UPHENO:0002267",
                    "UBERON:0010000",
                    "HP:0100261",
                    "BFO:0000040",
                    "UPHENO:0002581",
                    "BFO:0000040",
                    "UBERON:0000982",
                    "UPHENO:0002825",
                    "UPHENO:0046445",
                    "UPHENO:0069062",
                    "UPHENO:0046698",
                    "UBERON:0002204",
                    "UPHENO:0087888",
                    "UPHENO:0002816",
                    "UPHENO:0005092",
                    "UBERON:0001062",
                    "UBERON:0001015",
                    "UBERON:0001434",
                    "UBERON:0000383",
                    "UPHENO:0002699",
                    "UPHENO:0002964",
                    "UPHENO:0002525",
                    "HP:0011843",
                    "BFO:0000004",
                    "UBERON:0000043",
                    "UPHENO:0002698",
                    "UPHENO:0002385",
                    "UBERON:0034925",
                    "UBERON:0007846",
                    "HP:0034430",
                    "UPHENO:0002963",
                    "UPHENO:0046759",
                    "UBERON:0000465",
                    "UBERON:0011216",
                    "UBERON:0034921",
                    "UBERON:0004905",
                    "HP:0000001",
                    "HP:0034392",
                    "UPHENO:0002530",
                    "UPHENO:0069007",
                    "UPHENO:0002536",
                    "UPHENO:0046699",
                    "UPHENO:0081440",
                    "UPHENO:0076710",
                    "BFO:0000002",
                    "UBERON:0000467",
                    "UPHENO:0046706",
                    "UPHENO:0076692",
                    "BFO:0000001",
                    "UBERON:0000479",
                    "UPHENO:0001001",
                    "HP:0003549",
                    "HP:0011729",
                    "BFO:0000002",
                    "UPHENO:0003022",
                    "BFO:0000001",
                    "UBERON:0001630",
                    "UBERON:0011823",
                    "UBERON:0007845",
                ],
                "object_label": "Flexion contracture",
                "object_closure_label": [
                    "Abnormality of the musculoskeletal system",
                    "taxon specific phenotype",
                    "anatomical structure",
                    "muscle structure",
                    "decreased length of anatomical entity",
                    "organ phenotype",
                    "skeletal system morphology phenotype",
                    "multicellular organism phenotype",
                    "decreased length of material anatomical entity",
                    "anatomical entity morphology phenotype",
                    "material anatomical entity",
                    "articular system",
                    "musculoskeletal system",
                    "anatomical entity physiology phenotype",
                    "Phenotypic abnormality",
                    "decreased size of the anatomical structure",
                    "decreased length of regular connective tissue",
                    "organ system subdivision",
                    "multi organ part structure",
                    "Abnormality of connective tissue",
                    "Abnormality of joint mobility",
                    "Abnormal joint physiology",
                    "decreased length of multicellular anatomical structure",
                    "multicellular anatomical structure phenotype",
                    "organ system subdivision phenotype",
                    "entity",
                    "dense connective tissue",
                    "regular connective tissue",
                    "tendon morphology phenotype",
                    "size of anatomical entity phenotype",
                    "decreased length of tendon",
                    "musculoskeletal system phenotype",
                    "decreased size of the anatomical entity",
                    "phenotypic effect",
                    "independent continuant",
                    "tissue phenotype",
                    "decreased length of anatomical structure",
                    "All",
                    "Abnormality of the skeletal system",
                    "material anatomical entity phenotype",
                    "anatomical structure phenotype",
                    "Abnormal musculoskeletal physiology",
                    "tissue",
                    "phenotype",
                    "musculature phenotype",
                    "decreased length of dense connective tissue",
                    "anatomical structure physiology phenotype",
                    "multicellular anatomical structure",
                    "anatomical system physiology phenotype",
                    "muscle structure phenotype",
                    "skeletal system phenotype",
                    "musculature of body phenotype",
                    "organ",
                    "multicellular organism",
                    "articulation",
                    "tendon",
                    "decreased length of connective tissue",
                    "Abnormal tendon morphology",
                    "material entity",
                    "regular connective tissue phenotype",
                    "anatomical entity",
                    "Flexion contracture",
                    "Joint contracture",
                    "muscle organ phenotype",
                    "entity",
                    "anatomical system phenotype",
                    "decreased size of the connective tissue",
                    "anatomical entity phenotype",
                    "decreased length of dense regular connective tissue",
                    "musculoskeletal system physiology phenotype",
                    "muscle organ morphology phenotype",
                    "anatomical collection",
                    "musculature",
                    "skeletal system",
                    "musculature of body",
                    "skeletal joint",
                    "dense regular connective tissue phenotype",
                    "multicellular organism morphology phenotype",
                    "material entity",
                    "muscle organ",
                    "decreased length of tissue",
                    "decreased size of the multicellular anatomical structure",
                    "decreased size of the tissue",
                    "dense connective tissue phenotype",
                    "anatomical entity length phenotype",
                    "material anatomical entity physiology phenotype",
                    "continuant",
                    "anatomical system",
                    "connective tissue",
                    "dense regular connective tissue",
                    "Abnormal skeletal morphology",
                    "Abnormal skeletal muscle morphology",
                    "continuant",
                    "independent continuant",
                    "tendon phenotype",
                    "decreased size of the material anatomical entity",
                    "Abnormality of the musculature",
                    "connective tissue phenotype",
                    "anatomical entity",
                ],
                "object_taxon": None,
                "object_taxon_label": None,
                "primary_knowledge_source": "infores:hpo-annotations",
                "aggregator_knowledge_source": ["infores:monarchinitiative"],
                "negated": None,
                "pathway": None,
                "evidence_count": 1,
                "knowledge_level": "logical_entailment",
                "agent_type": "automated_agent",
                "has_evidence": None,
                "has_evidence_links": [],
                "has_count": None,
                "has_total": None,
                "has_percentage": None,
                "has_quotient": None,
                "grouping_key": "HGNC:27337||biolink:has_phenotype|HP:0001371",
                "provided_by": "hpoa_gene_to_phenotype_edges",
                "provided_by_link": {
                    "id": "hpoa_gene_to_phenotype",
                    "url": "https://monarch-initiative.github.io/monarch-ingest/Sources/hpoa/#gene_to_phenotype",
                },
                "publications": ["ORPHA:206549"],
                "publications_links": [{"id": "ORPHA:206549", "url": "http://identifiers.org/orphanet/206549"}],
                "frequency_qualifier": "HP:0040283",
                "onset_qualifier": None,
                "sex_qualifier": None,
                "stage_qualifier": None,
                "qualifiers": None,
                "qualifiers_label": None,
                "qualifiers_namespace": None,
                "qualifiers_category": None,
                "qualifier": None,
                "qualifier_label": None,
                "qualifier_namespace": None,
                "qualifier_category": None,
                "frequency_qualifier_label": "Occasional",
                "frequency_qualifier_namespace": "HP",
                "frequency_qualifier_category": "biolink:PhenotypicFeature",
                "onset_qualifier_label": None,
                "onset_qualifier_namespace": None,
                "onset_qualifier_category": None,
                "sex_qualifier_label": None,
                "sex_qualifier_namespace": None,
                "sex_qualifier_category": None,
                "stage_qualifier_label": None,
                "stage_qualifier_namespace": None,
                "stage_qualifier_category": None,
                "disease_context_qualifier": "MONDO:0012652",
                "disease_context_qualifier_label": "autosomal recessive limb-girdle muscular dystrophy type 2L",
                "disease_context_qualifier_namespace": "MONDO",
                "disease_context_qualifier_category": "biolink:Disease",
                "disease_context_qualifier_closure": [
                    "MONDO:0000429",
                    "MONDO:0016971",
                    "MONDO:0016106",
                    "MONDO:0100545",
                    "MONDO:0005336",
                    "MONDO:0005071",
                    "MONDO:0006025",
                    "MONDO:0020120",
                    "MONDO:0002081",
                    "MONDO:0000001",
                    "MONDO:0700223",
                    "MONDO:0012652",
                    "MONDO:0003847",
                    "MONDO:0020121",
                    "MONDO:0700096",
                    "MONDO:0100546",
                    "MONDO:0015152",
                    "MONDO:0019056",
                    "MONDO:0003939",
                ],
                "disease_context_qualifier_closure_label": [
                    "musculoskeletal system disorder",
                    "autosomal recessive limb-girdle muscular dystrophy",
                    "hereditary neuromuscular disease",
                    "human disease",
                    "hereditary disease",
                    "myopathy",
                    "limb-girdle muscular dystrophy",
                    "nervous system disorder",
                    "autosomal recessive disease",
                    "hereditary neurological disease",
                    "hereditary skeletal muscle disorder",
                    "autosomal recessive limb-girdle muscular dystrophy type 2L",
                    "autosomal genetic disease",
                    "neuromuscular disease",
                    "progressive muscular dystrophy",
                    "disease",
                    "muscular dystrophy",
                    "skeletal muscle disorder",
                    "muscle tissue disorder",
                ],
                "species_context_qualifier": None,
                "species_context_qualifier_label": None,
                "species_context_qualifier_namespace": None,
                "species_context_qualifier_category": None,
                "subject_specialization_qualifier": None,
                "subject_specialization_qualifier_label": None,
                "subject_specialization_qualifier_namespace": None,
                "subject_specialization_qualifier_category": None,
                "subject_specialization_qualifier_closure": None,
                "subject_specialization_qualifier_closure_label": None,
                "object_specialization_qualifier": None,
                "object_specialization_qualifier_label": None,
                "object_specialization_qualifier_namespace": None,
                "object_specialization_qualifier_category": None,
                "object_specialization_qualifier_closure": None,
                "object_specialization_qualifier_closure_label": None,
                "highlighting": None,
            },
            {
                "id": "uuid:11cb9476-198e-11f0-be82-6045bdb3d4c0",
                "category": "biolink:GeneToPhenotypicFeatureAssociation",
                "subject": "HGNC:27337",
                "original_subject": "NCBIGene:203859",
                "subject_namespace": "HGNC",
                "subject_category": "biolink:Gene",
                "subject_closure": None,
                "subject_label": "ANO5",
                "subject_closure_label": None,
                "subject_taxon": "NCBITaxon:9606",
                "subject_taxon_label": "Homo sapiens",
                "predicate": "biolink:has_phenotype",
                "original_predicate": None,
                "object": "HP:0009053",
                "original_object": None,
                "object_namespace": "HP",
                "object_category": "biolink:PhenotypicFeature",
                "object_closure": [
                    "UPHENO:0003095",
                    "UPHENO:0004467",
                    "HP:0009127",
                    "UPHENO:0003049",
                    "BFO:0000004",
                    "HP:0011804",
                    "BFO:0000002",
                    "UBERON:0000475",
                    "UBERON:0006058",
                    "UPHENO:0002320",
                    "HP:0002814",
                    "UPHENO:0003516",
                    "UPHENO:0003047",
                    "UPHENO:0002945",
                    "UPHENO:0080555",
                    "HP:0040064",
                    "HP:0009053",
                    "UBERON:0001062",
                    "UBERON:0002050",
                    "UBERON:0000062",
                    "UBERON:0010758",
                    "UPHENO:0082875",
                    "UPHENO:0003045",
                    "UPHENO:0003070",
                    "UPHENO:0002830",
                    "HP:0011805",
                    "UPHENO:0002949",
                    "UPHENO:0003081",
                    "UPHENO:0081581",
                    "UBERON:0005423",
                    "UBERON:0000468",
                    "UBERON:0010709",
                    "UBERON:0002101",
                    "UBERON:0004709",
                    "UBERON:0010890",
                    "HP:0003690",
                    "UPHENO:0003163",
                    "HP:0003011",
                    "UPHENO:0002536",
                    "UPHENO:0003432",
                    "UBERON:0000465",
                    "UBERON:0010707",
                    "UBERON:0004708",
                    "UBERON:0005420",
                    "UBERON:0004347",
                    "UBERON:0002529",
                    "UBERON:0000978",
                    "UBERON:0004480",
                    "UPHENO:0002847",
                    "UPHENO:0004456",
                    "UPHENO:0002526",
                    "HP:0000118",
                    "UPHENO:0002731",
                    "UPHENO:0002585",
                    "UPHENO:0002976",
                    "UBERON:0018254",
                    "UBERON:0005090",
                    "UBERON:0000922",
                    "UPHENO:0001002",
                    "UPHENO:0003334",
                    "HP:0033127",
                    "UPHENO:0002267",
                    "UPHENO:0002926",
                    "UBERON:0001062",
                    "UBERON:0006598",
                    "UBERON:0002103",
                    "HP:0007340",
                    "BFO:0000040",
                    "UPHENO:0003366",
                    "BFO:0000001",
                    "UBERON:0014892",
                    "UBERON:0007271",
                    "UBERON:0014792",
                    "UPHENO:0002944",
                    "BFO:0000002",
                    "UPHENO:0002897",
                    "UPHENO:0002359",
                    "UPHENO:0002568",
                    "UPHENO:0002861",
                    "UPHENO:0002816",
                    "UPHENO:0002386",
                    "UPHENO:0002571",
                    "UBERON:0001015",
                    "UBERON:0000383",
                    "UPHENO:0080575",
                    "UPHENO:0004900",
                    "UPHENO:0002747",
                    "UPHENO:0002541",
                    "UPHENO:0001003",
                    "UPHENO:0002525",
                    "BFO:0000004",
                    "UBERON:0010538",
                    "UBERON:0008784",
                    "UPHENO:0001001",
                    "UPHENO:0080556",
                    "HP:0002460",
                    "UPHENO:0002308",
                    "UPHENO:0002385",
                    "BFO:0000001",
                    "UBERON:0000061",
                    "UPHENO:0002963",
                    "UPHENO:0003065",
                    "UBERON:0010314",
                    "UBERON:0003102",
                    "UBERON:0010000",
                    "UBERON:0011216",
                    "HP:0000001",
                    "UPHENO:0003411",
                    "UPHENO:0002530",
                    "UPHENO:0076710",
                    "UBERON:0000467",
                    "RO:0002577",
                    "HP:0001324",
                    "UPHENO:0076692",
                    "BFO:0000040",
                    "UBERON:0004357",
                    "UBERON:0000026",
                    "UBERON:0000154",
                    "UPHENO:0003022",
                    "UPHENO:0002647",
                    "UBERON:0015212",
                    "UBERON:0001630",
                    "UBERON:0005418",
                ],
                "object_label": "Distal lower limb muscle weakness",
                "object_closure_label": [
                    "paired limb/fin bud phenotype",
                    "Abnormality of the musculoskeletal system",
                    "paired limb/fin segment phenotype",
                    "skeletal musculature",
                    "muscle structure",
                    "appendage girdle complex",
                    "paired limb/fin",
                    "subdivision of organism along appendicular axis",
                    "paired limb/fin segment",
                    "organ phenotype",
                    "continuant",
                    "skeletal muscle organ, vertebrate phenotype",
                    "anatomical entity morphology phenotype",
                    "entity",
                    "anatomical entity physiology phenotype",
                    "Phenotypic abnormality",
                    "lateral structure phenotype",
                    "decreased muscle organ strength",
                    "multicellular anatomical structure phenotype",
                    "organ system subdivision",
                    "appendage musculature phenotype",
                    "organ system subdivision phenotype",
                    "structure with developmental contribution from neural crest",
                    "surface structure",
                    "multicellular anatomical structure",
                    "hindlimb bud",
                    "limb segment phenotype",
                    "appendage phenotype",
                    "anatomical entity",
                    "embryonic structure",
                    "organism subdivision",
                    "limb segment",
                    "leg",
                    "musculature of limb",
                    "muscle organ physiology phenotype",
                    "Abnormality of the lower limb",
                    "phenotypic effect",
                    "developing anatomical structure",
                    "skeletal muscle organ, vertebrate",
                    "All",
                    "Limb muscle weakness",
                    "presumptive structure phenotype",
                    "material anatomical entity phenotype",
                    "limb bud phenotype",
                    "anatomical structure phenotype",
                    "paired limb/fin bud",
                    "appendage",
                    "posterior region of body",
                    "pelvic appendage phenotype",
                    "Muscle weakness",
                    "musculature phenotype",
                    "organ physiology phenotype",
                    "leg phenotype",
                    "anatomical structure physiology phenotype",
                    "multicellular organism",
                    "pelvic complex",
                    "limb",
                    "pelvic appendage",
                    "pelvic complex muscle",
                    "muscle structure phenotype",
                    "developing anatomical structure phenotype",
                    "musculature of body phenotype",
                    "limb phenotype",
                    "organ",
                    "lower limb segment",
                    "material entity",
                    "muscle structure physiology phenotype",
                    "Distal muscle weakness",
                    "multicellular anatomical structure physiology phenotype",
                    "presumptive structure",
                    "embryo",
                    "subdivision of organism along appendicular axis phenotype",
                    "hindlimb bud phenotype",
                    "hindlimb phenotype",
                    "muscle organ phenotype",
                    "multi-limb segment region phenotype",
                    "independent continuant",
                    "continuant",
                    "system",
                    "phenotype",
                    "paired limb/fin phenotype",
                    "decreased anatomical entity strength",
                    "anatomical system phenotype",
                    "muscle organ morphology phenotype",
                    "entity",
                    "anatomical structure",
                    "material entity",
                    "musculature",
                    "musculature of body",
                    "appendage musculature",
                    "musculature of pelvic complex",
                    "Lower limb muscle weakness",
                    "surface structure phenotype",
                    "multicellular organism phenotype",
                    "skeletal musculature phenotype",
                    "multicellular organism morphology phenotype",
                    "embryonic structure phenotype",
                    "Abnormal muscle physiology",
                    "muscle organ",
                    "pelvic appendage bud",
                    "limb bud",
                    "hindlimb",
                    "decreased pelvic complex muscle strength",
                    "embryo phenotype",
                    "Abnormality of the musculature of the limbs",
                    "anatomical entity phenotype",
                    "material anatomical entity physiology phenotype",
                    "organism subdivision phenotype",
                    "anatomical entity",
                    "anatomical system",
                    "Abnormal skeletal muscle morphology",
                    "lower limb segment phenotype",
                    "musculature of limb phenotype",
                    "material anatomical entity",
                    "independent continuant",
                    "multi-limb segment region",
                    "musculature of pelvic complex phenotype",
                    "pelvic appendage bud phenotype",
                    "Abnormality of the musculature",
                    "taxon specific phenotype",
                    "Abnormality of limbs",
                    "Distal lower limb muscle weakness",
                    "lateral structure",
                ],
                "object_taxon": None,
                "object_taxon_label": None,
                "primary_knowledge_source": "infores:hpo-annotations",
                "aggregator_knowledge_source": ["infores:monarchinitiative"],
                "negated": None,
                "pathway": None,
                "evidence_count": 1,
                "knowledge_level": "logical_entailment",
                "agent_type": "automated_agent",
                "has_evidence": None,
                "has_evidence_links": [],
                "has_count": None,
                "has_total": None,
                "has_percentage": None,
                "has_quotient": None,
                "grouping_key": "HGNC:27337||biolink:has_phenotype|HP:0009053",
                "provided_by": "hpoa_gene_to_phenotype_edges",
                "provided_by_link": {
                    "id": "hpoa_gene_to_phenotype",
                    "url": "https://monarch-initiative.github.io/monarch-ingest/Sources/hpoa/#gene_to_phenotype",
                },
                "publications": ["ORPHA:399096"],
                "publications_links": [{"id": "ORPHA:399096", "url": "http://identifiers.org/orphanet/399096"}],
                "frequency_qualifier": "HP:0040281",
                "onset_qualifier": None,
                "sex_qualifier": None,
                "stage_qualifier": None,
                "qualifiers": None,
                "qualifiers_label": None,
                "qualifiers_namespace": None,
                "qualifiers_category": None,
                "qualifier": None,
                "qualifier_label": None,
                "qualifier_namespace": None,
                "qualifier_category": None,
                "frequency_qualifier_label": "Very frequent",
                "frequency_qualifier_namespace": "HP",
                "frequency_qualifier_category": "biolink:PhenotypicFeature",
                "onset_qualifier_label": None,
                "onset_qualifier_namespace": None,
                "onset_qualifier_category": None,
                "sex_qualifier_label": None,
                "sex_qualifier_namespace": None,
                "sex_qualifier_category": None,
                "stage_qualifier_label": None,
                "stage_qualifier_namespace": None,
                "stage_qualifier_category": None,
                "disease_context_qualifier": "MONDO:0013222",
                "disease_context_qualifier_label": "Miyoshi muscular dystrophy 3",
                "disease_context_qualifier_namespace": "MONDO",
                "disease_context_qualifier_category": "biolink:Disease",
                "disease_context_qualifier_closure": [
                    "MONDO:0100545",
                    "MONDO:0005336",
                    "MONDO:0005071",
                    "MONDO:0020120",
                    "MONDO:0002081",
                    "MONDO:0013222",
                    "MONDO:0000001",
                    "MONDO:0700223",
                    "MONDO:0009685",
                    "MONDO:0003847",
                    "MONDO:0020121",
                    "MONDO:0018949",
                    "MONDO:0700096",
                    "MONDO:0100546",
                    "MONDO:0019056",
                    "MONDO:0003939",
                ],
                "disease_context_qualifier_closure_label": [
                    "musculoskeletal system disorder",
                    "hereditary neuromuscular disease",
                    "human disease",
                    "hereditary disease",
                    "myopathy",
                    "nervous system disorder",
                    "distal myopathy",
                    "hereditary neurological disease",
                    "hereditary skeletal muscle disorder",
                    "neuromuscular disease",
                    "Miyoshi muscular dystrophy 3",
                    "disease",
                    "muscular dystrophy",
                    "skeletal muscle disorder",
                    "Miyoshi myopathy",
                    "muscle tissue disorder",
                ],
                "species_context_qualifier": None,
                "species_context_qualifier_label": None,
                "species_context_qualifier_namespace": None,
                "species_context_qualifier_category": None,
                "subject_specialization_qualifier": None,
                "subject_specialization_qualifier_label": None,
                "subject_specialization_qualifier_namespace": None,
                "subject_specialization_qualifier_category": None,
                "subject_specialization_qualifier_closure": None,
                "subject_specialization_qualifier_closure_label": None,
                "object_specialization_qualifier": None,
                "object_specialization_qualifier_label": None,
                "object_specialization_qualifier_namespace": None,
                "object_specialization_qualifier_category": None,
                "object_specialization_qualifier_closure": None,
                "object_specialization_qualifier_closure_label": None,
                "highlighting": None,
            },
            {
                "id": "uuid:11cb9477-198e-11f0-be82-6045bdb3d4c0",
                "category": "biolink:GeneToPhenotypicFeatureAssociation",
                "subject": "HGNC:27337",
                "original_subject": "NCBIGene:203859",
                "subject_namespace": "HGNC",
                "subject_category": "biolink:Gene",
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                "subject_namespace": "HGNC",
                "subject_category": "biolink:Gene",
                "subject_closure": None,
                "subject_label": "RILPL1",
                "subject_closure_label": None,
                "subject_taxon": "NCBITaxon:9606",
                "subject_taxon_label": "Homo sapiens",
                "predicate": "biolink:has_phenotype",
                "original_predicate": None,
                "object": "HP:0002174",
                "original_object": None,
                "object_namespace": "HP",
                "object_category": "biolink:PhenotypicFeature",
                "object_closure": [
                    "UPHENO:0051267",
                    "UPHENO:0002577",
                    "UPHENO:0002433",
                    "UPHENO:0049708",
                    "UPHENO:0002949",
                    "BFO:0000004",
                    "UPHENO:0002554",
                    "UPHENO:0004969",
                    "BFO:0000002",
                    "BFO:0000003",
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                    "UBERON:0000307",
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                    "UBERON:0002329",
                    "UBERON:0000062",
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                    "UBERON:0005291",
                    "UBERON:0003104",
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                    "NBO:0000338",
                    "GO:0006936",
                    "GO:0050905",
                    "GO:0050882",
                    "UPHENO:0002269",
                    "UPHENO:0001002",
                    "UPHENO:0051293",
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                    "UPHENO:0001003",
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                    "UBERON:0006598",
                    "BFO:0000040",
                    "UPHENO:0002542",
                    "HP:0000707",
                    "BFO:0000001",
                    "BFO:0000015",
                    "BFO:0000040",
                    "GO:0008150",
                    "UBERON:0014892",
                    "GO:0003009",
                    "UPHENO:0003372",
                    "UPHENO:0002576",
                    "UPHENO:0049622",
                    "UPHENO:0051196",
                    "BFO:0000002",
                    "UPHENO:0005135",
                    "UPHENO:0002897",
                    "HP:0004305",
                    "UBERON:0001016",
                    "UBERON:0002385",
                    "GO:0007610",
                    "GO:0003008",
                    "GO:0050879",
                    "UPHENO:0083955",
                    "UPHENO:0002816",
                    "HP:0002174",
                    "UPHENO:0002571",
                    "UBERON:0001062",
                    "UBERON:0001015",
                    "UBERON:0000383",
                    "NBO:0000313",
                    "GO:0003012",
                    "GO:0050877",
                    "GO:0050881",
                    "GO:0003010",
                    "UPHENO:0004900",
                    "HP:0011442",
                    "HP:0100022",
                    "UPHENO:0002541",
                    "UPHENO:0004523",
                    "UPHENO:0003413",
                    "UPHENO:0002525",
                    "BFO:0000004",
                    "UPHENO:0003025",
                    "UPHENO:0049703",
                    "UPHENO:0079826",
                    "UPHENO:0002385",
                    "UBERON:0000061",
                    "UBERON:0034923",
                    "BFO:0000003",
                    "UPHENO:0002963",
                    "UPHENO:0003182",
                    "UBERON:0000465",
                    "UBERON:0010000",
                    "UBERON:0011216",
                    "NBO:0000001",
                    "GO:0006941",
                    "NBO:0000403",
                    "HP:0000001",
                    "UPHENO:0002530",
                    "UPHENO:0079833",
                    "UBERON:0000467",
                    "RO:0002577",
                    "GO:0032501",
                    "UPHENO:0002567",
                    "UBERON:0000479",
                    "UBERON:0013702",
                    "UPHENO:0001001",
                    "UPHENO:0003022",
                    "UPHENO:0005141",
                    "UBERON:0017650",
                    "UBERON:0015212",
                    "UBERON:0001630",
                    "UBERON:0009142",
                    "UBERON:0011676",
                    "UBERON:0013701",
                    "UBERON:0007503",
                    "UBERON:0000486",
                ],
                "object_label": "Postural tremor",
                "object_closure_label": [
                    "Tremor",
                    "subdivision of organism along main body axis phenotype",
                    "muscle system process phenotype",
                    "taxon specific phenotype",
                    "paraxial mesoderm phenotype",
                    "developing anatomical structure",
                    "skeletal musculature",
                    "presomitic mesoderm",
                    "mesoderm-derived structure",
                    "muscle structure",
                    "myotome",
                    "paraxial mesoderm",
                    "body part movement",
                    "striated muscle contraction",
                    "voluntary movement behavior",
                    "organ phenotype",
                    "voluntary skeletal muscle contraction phenotype",
                    "continuant",
                    "multilaminar epithelium phenotype",
                    "skeletal muscle organ, vertebrate phenotype",
                    "multicellular organism phenotype",
                    "entity",
                    "material anatomical entity",
                    "anatomical cluster",
                    "nervous system",
                    "muscle tissue",
                    "multicellular organismal process phenotype",
                    "anatomical entity physiology phenotype",
                    "Action tremor",
                    "Phenotypic abnormality",
                    "lateral structure phenotype",
                    "system process phenotype",
                    "organ system subdivision",
                    "behavior",
                    "system process",
                    "multicellular organismal movement",
                    "skeletal muscle contraction",
                    "muscle tissue phenotype",
                    "multicellular anatomical structure phenotype",
                    "myotome phenotype",
                    "organ system subdivision phenotype",
                    "multicellular anatomical structure",
                    "subdivision of organism along main body axis",
                    "main body axis",
                    "epithelial vesicle",
                    "multilaminar epithelium",
                    "biological_process in muscle organ phenotype",
                    "striated muscle contraction phenotype",
                    "entity",
                    "embryonic structure",
                    "somite",
                    "organism subdivision",
                    "phenotypic effect",
                    "skeletal muscle organ, vertebrate",
                    "behavior process",
                    "muscle system process",
                    "nervous system process",
                    "musculoskeletal movement",
                    "All",
                    "material anatomical entity phenotype",
                    "anatomical structure phenotype",
                    "tissue",
                    "body proper",
                    "kinesthetic behavior",
                    "muscle contraction",
                    "neuromuscular process",
                    "voluntary musculoskeletal movement",
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                    "musculature phenotype",
                    "Postural tremor",
                    "anatomical structure physiology phenotype",
                    "multicellular organism",
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                    "anatomical system physiology phenotype",
                    "muscle structure phenotype",
                    "developing anatomical structure phenotype",
                    "nervous system process phenotype",
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                    "musculature of body phenotype",
                    "presomitic mesoderm phenotype",
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                    "neuromuscular process phenotype",
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                    "organ",
                    "embryonic tissue phenotype",
                    "material entity",
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                    "behavior process phenotype",
                    "anatomical entity",
                    "presumptive structure",
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                    "epithelium phenotype",
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                    "continuant",
                    "occurrent",
                    "system",
                    "multicellular organismal process",
                    "presumptive paraxial mesoderm phenotype",
                    "trunk mesenchyme phenotype",
                    "anatomical system phenotype",
                    "voluntary movement behavior phenotype",
                    "anatomical structure",
                    "disconnected anatomical group",
                    "musculature",
                    "musculature of body",
                    "voluntary skeletal muscle contraction",
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                    "Abnormality of movement",
                    "skeletal musculature phenotype",
                    "embryonic structure phenotype",
                    "mesoderm-derived structure phenotype",
                    "epithelial vesicle phenotype",
                    "material entity",
                    "biological_process",
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                    "embryo phenotype",
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                    "mesenchyme phenotype",
                    "nervous system physiology phenotype",
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                    "nervous system phenotype",
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                    "material anatomical entity physiology phenotype",
                    "organism subdivision phenotype",
                    "anatomical system",
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                    "embryonic tissue",
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                    "presumptive structure phenotype",
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                    "skeletal muscle contraction phenotype",
                    "biological_process phenotype",
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                    "developing mesenchymal structure",
                    "lateral structure",
                    "trunk mesenchyme",
                    "dense mesenchyme tissue",
                    "trunk",
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                "object_taxon": None,
                "object_taxon_label": None,
                "primary_knowledge_source": "infores:hpo-annotations",
                "aggregator_knowledge_source": ["infores:monarchinitiative"],
                "negated": None,
                "pathway": None,
                "evidence_count": 1,
                "knowledge_level": "logical_entailment",
                "agent_type": "automated_agent",
                "has_evidence": None,
                "has_evidence_links": [],
                "has_count": 2,
                "has_total": 2,
                "has_percentage": 100.0,
                "has_quotient": 1.0,
                "grouping_key": "HGNC:26814||biolink:has_phenotype|HP:0002174",
                "provided_by": "hpoa_gene_to_phenotype_edges",
                "provided_by_link": {
                    "id": "hpoa_gene_to_phenotype",
                    "url": "https://monarch-initiative.github.io/monarch-ingest/Sources/hpoa/#gene_to_phenotype",
                },
                "publications": ["PMID:35148830"],
                "publications_links": [{"id": "PMID:35148830", "url": "http://identifiers.org/pubmed/35148830"}],
                "frequency_qualifier": None,
                "onset_qualifier": None,
                "sex_qualifier": None,
                "stage_qualifier": None,
                "qualifiers": None,
                "qualifiers_label": None,
                "qualifiers_namespace": None,
                "qualifiers_category": None,
                "qualifier": None,
                "qualifier_label": None,
                "qualifier_namespace": None,
                "qualifier_category": None,
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                "frequency_qualifier_namespace": None,
                "frequency_qualifier_category": None,
                "onset_qualifier_label": None,
                "onset_qualifier_namespace": None,
                "onset_qualifier_category": None,
                "sex_qualifier_label": None,
                "sex_qualifier_namespace": None,
                "sex_qualifier_category": None,
                "stage_qualifier_label": None,
                "stage_qualifier_namespace": None,
                "stage_qualifier_category": None,
                "disease_context_qualifier": "MONDO:0030712",
                "disease_context_qualifier_label": "oculopharyngodistal myopathy 4",
                "disease_context_qualifier_namespace": "MONDO",
                "disease_context_qualifier_category": "biolink:Disease",
                "disease_context_qualifier_closure": [
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                    "MONDO:0100545",
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                    "MONDO:0700096",
                    "MONDO:0100546",
                    "MONDO:0019056",
                    "MONDO:0003939",
                ],
                "disease_context_qualifier_closure_label": [
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                    "hereditary neuromuscular disease",
                    "human disease",
                    "hereditary disease",
                    "myopathy",
                    "nervous system disorder",
                    "distal myopathy",
                    "oculopharyngodistal myopathy 4",
                    "hereditary neurological disease",
                    "hereditary skeletal muscle disorder",
                    "neuromuscular disease",
                    "progressive muscular dystrophy",
                    "disease",
                    "oculopharyngodistal myopathy",
                    "muscular dystrophy",
                    "skeletal muscle disorder",
                    "muscle tissue disorder",
                ],
                "species_context_qualifier": None,
                "species_context_qualifier_label": None,
                "species_context_qualifier_namespace": None,
                "species_context_qualifier_category": None,
                "subject_specialization_qualifier": None,
                "subject_specialization_qualifier_label": None,
                "subject_specialization_qualifier_namespace": None,
                "subject_specialization_qualifier_category": None,
                "subject_specialization_qualifier_closure": None,
                "subject_specialization_qualifier_closure_label": None,
                "object_specialization_qualifier": None,
                "object_specialization_qualifier_label": None,
                "object_specialization_qualifier_namespace": None,
                "object_specialization_qualifier_category": None,
                "object_specialization_qualifier_closure": None,
                "object_specialization_qualifier_closure_label": None,
                "highlighting": None,
            },
        ],
        "facet_fields": [],
        "facet_queries": [],
    }
