Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B66b3bbba8252e4e0fb5091cf6b29833d> ?p ?o ?g. }
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- B66b3bbba8252e4e0fb5091cf6b29833d hasDbXref "NCIT:C36415" @default.
- B66b3bbba8252e4e0fb5091cf6b29833d hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B66b3bbba8252e4e0fb5091cf6b29833d hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B66b3bbba8252e4e0fb5091cf6b29833d type Axiom @default.
- B66b3bbba8252e4e0fb5091cf6b29833d annotatedProperty IAO_0000115 @default.
- B66b3bbba8252e4e0fb5091cf6b29833d annotatedSource MONDO_0100409 @default.
- B66b3bbba8252e4e0fb5091cf6b29833d annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(3;5)(q25;q34). (A cytogenetic abnormality that refers to the translocation of the long arm (q25) of chromosome 3 and the long arm (q34) of chromosome 5. It is associated with the development of acute myeloid leukemia arising from myelodysplastic syndrome, acute myeloid leukemia with multilineage dysplasia, and acute myeloid leukemia with myelodysplasia-related changes.)" @default.