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- NCIT_C132102 IAO_0000115 "A cytogenetic abnormality that refers to the translocation of chromosome 10p12 with chromosome 11q23. It is associated with acute myeloid leukemia in childhood." @default.
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- NCIT_C132102 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C132102 NCIT_P107 "t(10;11)(p12;q23)" @default.
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