Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Ba5d46ee690cb70d8c72a4c4f91ddfbb8> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Ba5d46ee690cb70d8c72a4c4f91ddfbb8 hasDbXref "DOID:0070065" @default.
- Ba5d46ee690cb70d8c72a4c4f91ddfbb8 type Axiom @default.
- Ba5d46ee690cb70d8c72a4c4f91ddfbb8 annotatedProperty IAO_0000115 @default.
- Ba5d46ee690cb70d8c72a4c4f91ddfbb8 annotatedSource MONDO_0014602 @default.
- Ba5d46ee690cb70d8c72a4c4f91ddfbb8 annotatedTarget "An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of PPP2R5D on chromosome 6p21.1." @default.