Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B76b7752b1888e3af1594cb8fa7cccb04> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B76b7752b1888e3af1594cb8fa7cccb04 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B76b7752b1888e3af1594cb8fa7cccb04 type Axiom @default.
- B76b7752b1888e3af1594cb8fa7cccb04 annotatedProperty IAO_0000115 @default.
- B76b7752b1888e3af1594cb8fa7cccb04 annotatedSource MONDO_0008519 @default.
- B76b7752b1888e3af1594cb8fa7cccb04 annotatedTarget "Any multiple synostoses syndrome in which the cause of the disease is a mutation in the NOG gene." @default.