Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B322c0bd204f28d1c0e6e9ec8754356dd> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B322c0bd204f28d1c0e6e9ec8754356dd hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B322c0bd204f28d1c0e6e9ec8754356dd type Axiom @default.
- B322c0bd204f28d1c0e6e9ec8754356dd annotatedProperty IAO_0000115 @default.
- B322c0bd204f28d1c0e6e9ec8754356dd annotatedSource MONDO_0011226 @default.
- B322c0bd204f28d1c0e6e9ec8754356dd annotatedTarget "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the POU4F3 gene." @default.