Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B0300a71790563dbb4bfbd0d8bde2e398> ?p ?o ?g. }
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- B0300a71790563dbb4bfbd0d8bde2e398 NCIT_P378 "NCI" @default.
- B0300a71790563dbb4bfbd0d8bde2e398 type Axiom @default.
- B0300a71790563dbb4bfbd0d8bde2e398 annotatedProperty IAO_0000115 @default.
- B0300a71790563dbb4bfbd0d8bde2e398 annotatedSource NCIT_C167194 @default.
- B0300a71790563dbb4bfbd0d8bde2e398 annotatedTarget "A cytogenetic abnormality that refers to the translocation of the short arm (p11.2) of chromosome 8 and the short arm (p13.3) of chromosome 16. It is associated with KAT6A/CREBBP fusions and acute myeloid leukemia." @default.