Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B73968dad98d6c09bb55dea362cb18ac3> ?p ?o ?g. }
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- B73968dad98d6c09bb55dea362cb18ac3 NCIT_P378 "NCI" @default.
- B73968dad98d6c09bb55dea362cb18ac3 type Axiom @default.
- B73968dad98d6c09bb55dea362cb18ac3 annotatedProperty IAO_0000115 @default.
- B73968dad98d6c09bb55dea362cb18ac3 annotatedSource NCIT_C36372 @default.
- B73968dad98d6c09bb55dea362cb18ac3 annotatedTarget "A cytogenetic abnormality that refers to the translocation of the long arm (q23.3) of chromosome 11 and the short arm (p13.3) of chromosome 19. It is associated with KMT2A (MLL)/MLLT1 (ENL) fusions and acute myeloid leukemia." @default.