Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bb43d35812af8237686f635cb16ec9c9b> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bb43d35812af8237686f635cb16ec9c9b NCIT_P378 "NCI" @default.
- Bb43d35812af8237686f635cb16ec9c9b type Axiom @default.
- Bb43d35812af8237686f635cb16ec9c9b annotatedProperty IAO_0000115 @default.
- Bb43d35812af8237686f635cb16ec9c9b annotatedSource NCIT_C36631 @default.
- Bb43d35812af8237686f635cb16ec9c9b annotatedTarget "A cytogenetic abnormality that refers to loss of all or part of chromosome 17." @default.