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- NCIT_C177207 IAO_0000115 "A cytogenetic abnormality that involves a translocation between chromosomes 6 and 14." @default.
- NCIT_C177207 NCIT_NHC0 "C177207" @default.
- NCIT_C177207 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C177207 NCIT_P108 "t(6;14)" @default.
- NCIT_C177207 NCIT_P208 "CL1643027" @default.
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- NCIT_C177207 NCIT_R173 NCIT_C13209 @default.
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- NCIT_C177207 NCIT_R173 NCIT_C13404 @default.
- NCIT_C177207 NCIT_R173 NCIT_C14134 @default.
- NCIT_C177207 NCIT_R173 NCIT_C21599 @default.
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- NCIT_C177207 referenceCount "1" @default.
- NCIT_C177207 hasExactSynonym "t(6;14)" @default.
- NCIT_C177207 type Class @default.
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- NCIT_C177207 label "t(6;14)" @default.
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