Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc3a2c63dc821bce8857f3cf5db29b8fe> ?p ?o ?g. }
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- Bc3a2c63dc821bce8857f3cf5db29b8fe hasDbXref "NCIT:C168764" @default.
- Bc3a2c63dc821bce8857f3cf5db29b8fe hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Bc3a2c63dc821bce8857f3cf5db29b8fe hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Bc3a2c63dc821bce8857f3cf5db29b8fe type Axiom @default.
- Bc3a2c63dc821bce8857f3cf5db29b8fe annotatedProperty IAO_0000115 @default.
- Bc3a2c63dc821bce8857f3cf5db29b8fe annotatedSource MONDO_0100383 @default.
- Bc3a2c63dc821bce8857f3cf5db29b8fe annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23;p13). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13) of chromosome 19. It is associated with KMT2A (MLL) fusions, including those with MLLT1 (ENL) and ELL, and acute myeloid leukemia.)" @default.