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- NCIT_C128654 IAO_0000115 "A cytogenetic abnormality that involves a translocation between chromosomes 1 and 19." @default.
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- NCIT_C128654 NCIT_P106 "Cell or Molecular Dysfunction" @default.
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- NCIT_C128654 NCIT_P208 "CL509586" @default.
- NCIT_C128654 NCIT_P322 "CTRP" @default.
- NCIT_C128654 NCIT_P322 "PCDC" @default.
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- NCIT_C128654 NCIT_R173 NCIT_C13202 @default.
- NCIT_C128654 NCIT_R173 NCIT_C13203 @default.
- NCIT_C128654 NCIT_R173 NCIT_C13204 @default.
- NCIT_C128654 NCIT_R173 NCIT_C13214 @default.
- NCIT_C128654 NCIT_R173 NCIT_C13404 @default.
- NCIT_C128654 NCIT_R173 NCIT_C14134 @default.
- NCIT_C128654 NCIT_R173 NCIT_C21599 @default.
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- NCIT_C128654 hasExactSynonym "t(1;19)" @default.
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- NCIT_C128654 type Class @default.
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- NCIT_C128654 label "t(1;19)" @default.
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