Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B78ccb0fc816f6e5b9b7037b38c660f59> ?p ?o ?g. }
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- B78ccb0fc816f6e5b9b7037b38c660f59 hasDbXref "NCIT:C131503" @default.
- B78ccb0fc816f6e5b9b7037b38c660f59 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B78ccb0fc816f6e5b9b7037b38c660f59 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B78ccb0fc816f6e5b9b7037b38c660f59 type Axiom @default.
- B78ccb0fc816f6e5b9b7037b38c660f59 annotatedProperty IAO_0000115 @default.
- B78ccb0fc816f6e5b9b7037b38c660f59 annotatedSource MONDO_0100395 @default.
- B78ccb0fc816f6e5b9b7037b38c660f59 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(5;11)(q35;p15). (A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 5q35. It results in the formation of NUP98/NSD1 fusion gene. It is associated with the development of acute myeloid leukemia with t(5;11)(q35;p15); NUP98-NSD1.)" @default.