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- NCIT_C168766 IAO_0000115 "A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 3 and the short arm (p12.3) of chromosome 12. It is associated with ETV6/MECOM (EVI1) fusions, myeloproliferative disorders, myelodysplastic syndromes and acute myelogenous leukemia." @default.
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- NCIT_C168766 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C168766 NCIT_P108 "t(3;12)(q23;p12.3)" @default.
- NCIT_C168766 NCIT_P208 "CL1378673" @default.
- NCIT_C168766 NCIT_P322 "PCDC" @default.
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- NCIT_C168766 NCIT_R177 NCIT_C28510 @default.
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- NCIT_C168766 normalizedInformationContent "100" @default.
- NCIT_C168766 referenceCount "1" @default.
- NCIT_C168766 hasExactSynonym "t(3;12)(q23;p12.3)" @default.
- NCIT_C168766 inSubset NCIT_C173233 @default.
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- NCIT_C168766 type Class @default.
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- NCIT_C168766 label "t(3;12)(q23;p12.3)" @default.
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- NCIT_C168766 subClassOf NCIT_C97926 @default.