Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B4cf9bf8073efc2a0f301d9c69ee2cdc5> ?p ?o ?g. }
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- B4cf9bf8073efc2a0f301d9c69ee2cdc5 NCIT_P378 "NCI" @default.
- B4cf9bf8073efc2a0f301d9c69ee2cdc5 type Axiom @default.
- B4cf9bf8073efc2a0f301d9c69ee2cdc5 annotatedProperty IAO_0000115 @default.
- B4cf9bf8073efc2a0f301d9c69ee2cdc5 annotatedSource NCIT_C36597 @default.
- B4cf9bf8073efc2a0f301d9c69ee2cdc5 annotatedTarget "A cytogenetic abnormality that refers to loss of all or part of chromosome 1." @default.