Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5cccd022a6ca81d00a05646ba0024e05> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B5cccd022a6ca81d00a05646ba0024e05 NCIT_P378 "NCI" @default.
- B5cccd022a6ca81d00a05646ba0024e05 type Axiom @default.
- B5cccd022a6ca81d00a05646ba0024e05 annotatedProperty IAO_0000115 @default.
- B5cccd022a6ca81d00a05646ba0024e05 annotatedSource NCIT_C36632 @default.
- B5cccd022a6ca81d00a05646ba0024e05 annotatedTarget "A cytogenetic abnormality that refers to loss of all or part of chromosome 19." @default.