Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B71eef0df05a78f82eceee679a458f0f5> ?p ?o ?g. }
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- B71eef0df05a78f82eceee679a458f0f5 hasDbXref "NCIT:C36371" @default.
- B71eef0df05a78f82eceee679a458f0f5 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B71eef0df05a78f82eceee679a458f0f5 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B71eef0df05a78f82eceee679a458f0f5 type Axiom @default.
- B71eef0df05a78f82eceee679a458f0f5 annotatedProperty IAO_0000115 @default.
- B71eef0df05a78f82eceee679a458f0f5 annotatedSource MONDO_0100384 @default.
- B71eef0df05a78f82eceee679a458f0f5 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.