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- Bddd99bf00955edeffcaff2f7e8ec2e2e hasDbXref "NCIT:C168764" @default.
- Bddd99bf00955edeffcaff2f7e8ec2e2e hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Bddd99bf00955edeffcaff2f7e8ec2e2e hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Bddd99bf00955edeffcaff2f7e8ec2e2e type Axiom @default.
- Bddd99bf00955edeffcaff2f7e8ec2e2e annotatedProperty IAO_0000115 @default.
- Bddd99bf00955edeffcaff2f7e8ec2e2e annotatedSource MONDO_0100383 @default.
- Bddd99bf00955edeffcaff2f7e8ec2e2e annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23;p13). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13) of chromosome 19. It is associated with KMT2A (MLL) fusions, including those with MLLT1 (ENL) and ELL, and acute myeloid leukemia.)" @default.