Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B0a01b6c190e92dd1b44deddf6ef287a2> ?p ?o ?g. }
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- B0a01b6c190e92dd1b44deddf6ef287a2 NCIT_P378 "NCI" @default.
- B0a01b6c190e92dd1b44deddf6ef287a2 type Axiom @default.
- B0a01b6c190e92dd1b44deddf6ef287a2 annotatedProperty IAO_0000115 @default.
- B0a01b6c190e92dd1b44deddf6ef287a2 annotatedSource NCIT_C36549 @default.
- B0a01b6c190e92dd1b44deddf6ef287a2 annotatedTarget "A cytogenetic abnormality that refers to loss of all or part of chromosome 11." @default.