Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be5310b51795d4d96e60f53d77c6c5fdc> ?p ?o ?g. }
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- Be5310b51795d4d96e60f53d77c6c5fdc hasDbXref "NCIT:C36372" @default.
- Be5310b51795d4d96e60f53d77c6c5fdc hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Be5310b51795d4d96e60f53d77c6c5fdc hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Be5310b51795d4d96e60f53d77c6c5fdc type Axiom @default.
- Be5310b51795d4d96e60f53d77c6c5fdc annotatedProperty IAO_0000115 @default.
- Be5310b51795d4d96e60f53d77c6c5fdc annotatedSource MONDO_0100385 @default.
- Be5310b51795d4d96e60f53d77c6c5fdc annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23.3;p13.3). (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.