Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bd763f86c6e52084bc0c48a3bd2ac7471> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bd763f86c6e52084bc0c48a3bd2ac7471 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- Bd763f86c6e52084bc0c48a3bd2ac7471 type Axiom @default.
- Bd763f86c6e52084bc0c48a3bd2ac7471 annotatedProperty IAO_0000115 @default.
- Bd763f86c6e52084bc0c48a3bd2ac7471 annotatedSource MONDO_0010398 @default.
- Bd763f86c6e52084bc0c48a3bd2ac7471 annotatedTarget "Any X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the UPF3B gene." @default.