Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8baea7a58979f9f44a59a85f5aca2aef> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B8baea7a58979f9f44a59a85f5aca2aef hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B8baea7a58979f9f44a59a85f5aca2aef type Axiom @default.
- B8baea7a58979f9f44a59a85f5aca2aef annotatedProperty IAO_0000115 @default.
- B8baea7a58979f9f44a59a85f5aca2aef annotatedSource MONDO_0013963 @default.
- B8baea7a58979f9f44a59a85f5aca2aef annotatedTarget "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CABP2 gene." @default.