Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B68aa891d20cfab01dccd5a0c747cee58> ?p ?o ?g. }
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- B68aa891d20cfab01dccd5a0c747cee58 NCIT_P378 "NCI" @default.
- B68aa891d20cfab01dccd5a0c747cee58 type Axiom @default.
- B68aa891d20cfab01dccd5a0c747cee58 annotatedProperty IAO_0000115 @default.
- B68aa891d20cfab01dccd5a0c747cee58 annotatedSource NCIT_C36463 @default.
- B68aa891d20cfab01dccd5a0c747cee58 annotatedTarget "A cytogenetic abnormality that refers to the allelic gain of all or part of chromosome 9." @default.