Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bdd1c8de1eee14da4fe1c3bcf3aff2a78> ?p ?o ?g. }
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- Bdd1c8de1eee14da4fe1c3bcf3aff2a78 hasDbXref "NCIT:C168758" @default.
- Bdd1c8de1eee14da4fe1c3bcf3aff2a78 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Bdd1c8de1eee14da4fe1c3bcf3aff2a78 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Bdd1c8de1eee14da4fe1c3bcf3aff2a78 type Axiom @default.
- Bdd1c8de1eee14da4fe1c3bcf3aff2a78 annotatedProperty IAO_0000115 @default.
- Bdd1c8de1eee14da4fe1c3bcf3aff2a78 annotatedSource MONDO_0100378 @default.
- Bdd1c8de1eee14da4fe1c3bcf3aff2a78 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(10;11)(p11.2;q23). (A cytogenetic abnormality that refers to the translocation of the short arm (p11.2) of chromosome 10 and the long arm (q23) of chromosome 11. It is associated with KMT2A (MLL)/ABI1 fusions and acute myeloid leukemia.)" @default.