Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B334488a2d6a87d8a15e2b4d29df9f2cd> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B334488a2d6a87d8a15e2b4d29df9f2cd NCIT_P378 "NCI" @default.
- B334488a2d6a87d8a15e2b4d29df9f2cd type Axiom @default.
- B334488a2d6a87d8a15e2b4d29df9f2cd annotatedProperty IAO_0000115 @default.
- B334488a2d6a87d8a15e2b4d29df9f2cd annotatedSource NCIT_C36597 @default.
- B334488a2d6a87d8a15e2b4d29df9f2cd annotatedTarget "A cytogenetic abnormality that refers to loss of all or part of chromosome 1." @default.