Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B6083fbeeb195e9832977d167b84ed551> ?p ?o ?g. }
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- B6083fbeeb195e9832977d167b84ed551 hasDbXref "NCIT:C67495" @default.
- B6083fbeeb195e9832977d167b84ed551 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B6083fbeeb195e9832977d167b84ed551 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B6083fbeeb195e9832977d167b84ed551 type Axiom @default.
- B6083fbeeb195e9832977d167b84ed551 annotatedProperty IAO_0000115 @default.
- B6083fbeeb195e9832977d167b84ed551 annotatedSource MONDO_0100416 @default.
- B6083fbeeb195e9832977d167b84ed551 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly FLT3 tyrosine kinase domain point mutation. (Single nucleotide mutations in the tyrosine kinase domain encoded by the human FLT3 gene that are associated with acute myeloid leukemia and poor prognosis.)" @default.