a sequence variant in which the allele state is associated in some way with the disease state
URI: biolink:variant_to_disease_association_subject
VariantToDiseaseAssociation → 1..1 NamedThing
| Local names: | annotation subject (ga4gh) | |
| node with outgoing relationship (neo4j) | ||
| Mappings: | rdf:subject | |
| Examples: | Example(value=’CLINVAR:52241’, description=’NM_000059.3(BRCA2):c.7007G>C (p.Arg2336Pro)’, object=None) | |
| Exact Mappings: | owl:annotatedSource | |
| OBAN:association_has_subject |