Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be2346050a8f411d25eed9c01a9d583be> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Be2346050a8f411d25eed9c01a9d583be NCIT_P378 "NCI" @default.
- Be2346050a8f411d25eed9c01a9d583be type Axiom @default.
- Be2346050a8f411d25eed9c01a9d583be annotatedProperty IAO_0000115 @default.
- Be2346050a8f411d25eed9c01a9d583be annotatedSource NCIT_C129035 @default.
- Be2346050a8f411d25eed9c01a9d583be annotatedTarget "An autosomal dominant disorder caused by mutation(s) in the ANKRD26 gene, encoding ANKRD26 protein. Additionally, in one family, a mutation(s) has been identified in the MASTL gene, encoding serine/threonine-protein kinase greatwall. The condition is characterized by mild to moderate bruisability." @default.