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- B0106eeeb7f6fb63442628cae1b256353 hasDbXref "NCIT:C168773" @default.
- B0106eeeb7f6fb63442628cae1b256353 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B0106eeeb7f6fb63442628cae1b256353 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B0106eeeb7f6fb63442628cae1b256353 type Axiom @default.
- B0106eeeb7f6fb63442628cae1b256353 annotatedProperty IAO_0000115 @default.
- B0106eeeb7f6fb63442628cae1b256353 annotatedSource MONDO_0100408 @default.
- B0106eeeb7f6fb63442628cae1b256353 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(16;21)(q24;q22). (A cytogenetic abnormality that refers to the translocation of the long arm (q24) of chromosome 16 and the long arm (q22) of chromosome 22. It is associated with RUNX1/CBFA2T3 fusions, myelodysplastic syndromes and acute myeloid leukemia.)" @default.