Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bb0d90850d81f3b22651e68f90dfe5ea6> ?p ?o ?g. }
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- Bb0d90850d81f3b22651e68f90dfe5ea6 hasDbXref "NCIT:C168766" @default.
- Bb0d90850d81f3b22651e68f90dfe5ea6 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Bb0d90850d81f3b22651e68f90dfe5ea6 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Bb0d90850d81f3b22651e68f90dfe5ea6 type Axiom @default.
- Bb0d90850d81f3b22651e68f90dfe5ea6 annotatedProperty IAO_0000115 @default.
- Bb0d90850d81f3b22651e68f90dfe5ea6 annotatedSource MONDO_0100400 @default.
- Bb0d90850d81f3b22651e68f90dfe5ea6 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(3;12)(q23;p12.3). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 3 and the short arm (p12.3) of chromosome 12. It is associated with ETV6/MECOM (EVI1) fusions, myeloproliferative disorders, myelodysplastic syndromes and acute myelogenous leukemia.)" @default.