Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B216ea190d70a8b16b8a19e4bcdad6512> ?p ?o ?g. }
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- B216ea190d70a8b16b8a19e4bcdad6512 hasDbXref "NCIT:C36370" @default.
- B216ea190d70a8b16b8a19e4bcdad6512 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B216ea190d70a8b16b8a19e4bcdad6512 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B216ea190d70a8b16b8a19e4bcdad6512 type Axiom @default.
- B216ea190d70a8b16b8a19e4bcdad6512 annotatedProperty IAO_0000115 @default.
- B216ea190d70a8b16b8a19e4bcdad6512 annotatedSource MONDO_0100376 @default.
- B216ea190d70a8b16b8a19e4bcdad6512 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.