Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B62f16bf893f0a06e6a0aba38b4273c2a> ?p ?o ?g. }
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- B62f16bf893f0a06e6a0aba38b4273c2a hasDbXref "NCIT:C168773" @default.
- B62f16bf893f0a06e6a0aba38b4273c2a hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B62f16bf893f0a06e6a0aba38b4273c2a hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B62f16bf893f0a06e6a0aba38b4273c2a type Axiom @default.
- B62f16bf893f0a06e6a0aba38b4273c2a annotatedProperty IAO_0000115 @default.
- B62f16bf893f0a06e6a0aba38b4273c2a annotatedSource MONDO_0100408 @default.
- B62f16bf893f0a06e6a0aba38b4273c2a 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.