Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf1d0b8c2bf597931377fb5f39ee00192> ?p ?o ?g. }
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- Bf1d0b8c2bf597931377fb5f39ee00192 hasDbXref "NCIT:C36370" @default.
- Bf1d0b8c2bf597931377fb5f39ee00192 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Bf1d0b8c2bf597931377fb5f39ee00192 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Bf1d0b8c2bf597931377fb5f39ee00192 type Axiom @default.
- Bf1d0b8c2bf597931377fb5f39ee00192 annotatedProperty IAO_0000115 @default.
- Bf1d0b8c2bf597931377fb5f39ee00192 annotatedSource MONDO_0100376 @default.
- Bf1d0b8c2bf597931377fb5f39ee00192 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(9;11)(p21.3;q23.3). (A cytogenetic abnormality that refers to the translocation of the short arm (p21.3) of chromosome 9 and the long arm (q23.3) of chromosome 11. It is associated with the development of acute myeloid leukemia with the MLLT3-MLL fusion gene transcript.)" @default.