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- NCIT_C67495 IAO_0000115 "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.
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- NCIT_C67495 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C67495 NCIT_P107 "FLT3 Tyrosine Kinase Domain Point Mutation" @default.
- NCIT_C67495 NCIT_P108 "FLT3 Tyrosine Kinase Domain Point Mutation" @default.
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- NCIT_C67495 NCIT_P322 "CTRP" @default.
- NCIT_C67495 NCIT_P322 "PCDC" @default.
- NCIT_C67495 NCIT_P366 "FLT3_Tyrosine_Kinase_Domain_Point_Mutation" @default.
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- NCIT_C67495 normalizedInformationContent "92.730304365937428" @default.
- NCIT_C67495 referenceCount "3" @default.
- NCIT_C67495 hasExactSynonym "FLT3 Tyrosine Kinase Domain Point Mutation" @default.
- NCIT_C67495 hasExactSynonym "FLT3-TKD Point Mutation" @default.
- NCIT_C67495 hasExactSynonym "FLT3/TKD Point Mutation" @default.
- NCIT_C67495 inSubset NCIT_C116977 @default.
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- NCIT_C67495 type Class @default.
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- NCIT_C67495 label "FLT3 Tyrosine Kinase Domain Point Mutation" @default.
- NCIT_C67495 subClassOf NCIT_C120063 @default.
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