Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B78b8a4adb4ebd003a6943bbfd15f89b9> ?p ?o ?g. }
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- B78b8a4adb4ebd003a6943bbfd15f89b9 NCIT_P378 "NCI" @default.
- B78b8a4adb4ebd003a6943bbfd15f89b9 type Axiom @default.
- B78b8a4adb4ebd003a6943bbfd15f89b9 annotatedProperty IAO_0000115 @default.
- B78b8a4adb4ebd003a6943bbfd15f89b9 annotatedSource NCIT_C36439 @default.
- B78b8a4adb4ebd003a6943bbfd15f89b9 annotatedTarget "A cytogenetic abnormality that refers to the duplication of all or part of the short arm of chromosome 2." @default.