Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc2cf80cd7d262fa47aa862289a7e60b3> ?p ?o ?g. }
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- Bc2cf80cd7d262fa47aa862289a7e60b3 hasDbXref "NCIT:C168759" @default.
- Bc2cf80cd7d262fa47aa862289a7e60b3 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Bc2cf80cd7d262fa47aa862289a7e60b3 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Bc2cf80cd7d262fa47aa862289a7e60b3 type Axiom @default.
- Bc2cf80cd7d262fa47aa862289a7e60b3 annotatedProperty IAO_0000115 @default.
- Bc2cf80cd7d262fa47aa862289a7e60b3 annotatedSource MONDO_0100379 @default.
- Bc2cf80cd7d262fa47aa862289a7e60b3 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(1;11)(q21;q23). (A cytogenetic abnormality that refers to the translocation of the long arm (q21) of chromosome 1 and the long arm (q23) of chromosome 11. It is associated with KMT2A (MLL)/MLLT11 (AF1Q) fusions, acute myeloid leukemia and some cases of acute lymphoblastic leukemia.)" @default.