Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B924dbaf3027be545f2e89455f4fd2501> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B924dbaf3027be545f2e89455f4fd2501 NCIT_P378 "NCI" @default.
- B924dbaf3027be545f2e89455f4fd2501 type Axiom @default.
- B924dbaf3027be545f2e89455f4fd2501 annotatedProperty IAO_0000115 @default.
- B924dbaf3027be545f2e89455f4fd2501 annotatedSource NCIT_C41371 @default.
- B924dbaf3027be545f2e89455f4fd2501 annotatedTarget "A cytogenetic abnormality that refers to loss of all or part of chromosome 12." @default.