Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B660ee057666cc6a0d02c4732f3e003b1> ?p ?o ?g. }
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- B660ee057666cc6a0d02c4732f3e003b1 hasDbXref "NCIT:C36532" @default.
- B660ee057666cc6a0d02c4732f3e003b1 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B660ee057666cc6a0d02c4732f3e003b1 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B660ee057666cc6a0d02c4732f3e003b1 type Axiom @default.
- B660ee057666cc6a0d02c4732f3e003b1 annotatedProperty IAO_0000115 @default.
- B660ee057666cc6a0d02c4732f3e003b1 annotatedSource MONDO_0100382 @default.
- B660ee057666cc6a0d02c4732f3e003b1 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(6;9)(p23;q34.1). (A cytogenetic abnormality that refers to the translocation of the short arm (p23) of chromosome 6 and the long arm (q34.1) of chromosome 9. It is associated with DEK/NUP214 fusions, acute myeloid leukemia and myelodysplastic syndromes.)" @default.