Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B4d20d12a81f641dbe5573cc61579acec> ?p ?o ?g. }
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- B4d20d12a81f641dbe5573cc61579acec hasDbXref "NCIT:C36371" @default.
- B4d20d12a81f641dbe5573cc61579acec hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B4d20d12a81f641dbe5573cc61579acec hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B4d20d12a81f641dbe5573cc61579acec type Axiom @default.
- B4d20d12a81f641dbe5573cc61579acec annotatedProperty IAO_0000115 @default.
- B4d20d12a81f641dbe5573cc61579acec annotatedSource MONDO_0100384 @default.
- B4d20d12a81f641dbe5573cc61579acec annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23;p13.1). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13.1) of chromosome 19. It is associated with the development of acute myeloid leukemia with variant MLL translocations and topoisomerase II inhibitor-related acute myeloid leukemia.)" @default.