Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bbdac5a9a44ce2b6d271be7dc8e96c37d> ?p ?o ?g. }
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- Bbdac5a9a44ce2b6d271be7dc8e96c37d hasDbXref "NCIT:C36373" @default.
- Bbdac5a9a44ce2b6d271be7dc8e96c37d hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Bbdac5a9a44ce2b6d271be7dc8e96c37d hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Bbdac5a9a44ce2b6d271be7dc8e96c37d type Axiom @default.
- Bbdac5a9a44ce2b6d271be7dc8e96c37d annotatedProperty IAO_0000115 @default.
- Bbdac5a9a44ce2b6d271be7dc8e96c37d annotatedSource MONDO_0100373 @default.
- Bbdac5a9a44ce2b6d271be7dc8e96c37d annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly inv(16)(p13.1;q22). (A chromosomal inversion that involves chromosome 16. It is associated with the development of acute myeloid leukemia CBFB-MYH11, acute myelomonocytic leukemia with abnormal eosinophils, and granulocytic sarcoma.)" @default.