Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf6535aeea5a48a6983b9444f8bd6b8b3> ?p ?o ?g. }
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- Bf6535aeea5a48a6983b9444f8bd6b8b3 hasDbXref "NCIT:C67495" @default.
- Bf6535aeea5a48a6983b9444f8bd6b8b3 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Bf6535aeea5a48a6983b9444f8bd6b8b3 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Bf6535aeea5a48a6983b9444f8bd6b8b3 type Axiom @default.
- Bf6535aeea5a48a6983b9444f8bd6b8b3 annotatedProperty IAO_0000115 @default.
- Bf6535aeea5a48a6983b9444f8bd6b8b3 annotatedSource MONDO_0100416 @default.
- Bf6535aeea5a48a6983b9444f8bd6b8b3 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.