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- B01eb43ab438173e19f4938d40d609dc3 NCIT_P378 "NCI" @default.
- B01eb43ab438173e19f4938d40d609dc3 type Axiom @default.
- B01eb43ab438173e19f4938d40d609dc3 annotatedProperty IAO_0000115 @default.
- B01eb43ab438173e19f4938d40d609dc3 annotatedSource NCIT_C13727 @default.
- B01eb43ab438173e19f4938d40d609dc3 annotatedTarget "A translocation between chromosomes 12 and 21 involved in TEL-AML1 oncogene formation. The translocation produces a chimeric gene encoding a protein consisting of the N-terminal HLH domain of the TEL ETS-like transcription factor fused with a nearly complete AML1 protein. t(12;21) is the most frequent translocation causing ALL, accounting for 20% of ALL cases." @default.