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- NCIT_C120223 IAO_0000115 "A cytogenetic abnormality that refers to the translocation involving the genes CIC (capicua transcriptional suppressor) on chromosome 19 and DUX4L (double homeobox 4-like) on chromosome 10 resulting in CIC-DUX4L fusion." @default.
- NCIT_C120223 NCIT_A28 NCIT_C3910 @default.
- NCIT_C120223 NCIT_NHC0 "C120223" @default.
- NCIT_C120223 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C120223 NCIT_P108 "t(10;19)(q26;q13)" @default.
- NCIT_C120223 NCIT_P207 "C3897143" @default.
- NCIT_C120223 NCIT_P322 "PCDC" @default.
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- NCIT_C120223 NCIT_R173 NCIT_C13202 @default.
- NCIT_C120223 NCIT_R173 NCIT_C13203 @default.
- NCIT_C120223 NCIT_R173 NCIT_C13205 @default.
- NCIT_C120223 NCIT_R173 NCIT_C13214 @default.
- NCIT_C120223 NCIT_R173 NCIT_C13404 @default.
- NCIT_C120223 NCIT_R173 NCIT_C14134 @default.
- NCIT_C120223 NCIT_R173 NCIT_C21599 @default.
- NCIT_C120223 NCIT_R177 NCIT_C165670 @default.
- NCIT_C120223 NCIT_R177 NCIT_C16612 @default.
- NCIT_C120223 NCIT_R177 NCIT_C28510 @default.
- NCIT_C120223 NCIT_R177 NCIT_C54362 @default.
- NCIT_C120223 NCIT_R177 NCIT_C97912 @default.
- NCIT_C120223 normalizedInformationContent "90.826665450122817" @default.
- NCIT_C120223 referenceCount "4" @default.
- NCIT_C120223 hasExactSynonym "t(10;19)(q26;q13)" @default.
- NCIT_C120223 inSubset NCIT_C174237 @default.
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- NCIT_C120223 type Class @default.
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- NCIT_C120223 label "t(10;19)(q26;q13)" @default.
- NCIT_C120223 subClassOf B3d55611f287ed3693d2ebc3bebd69d67 @default.
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- NCIT_C120223 subClassOf NCIT_C2950 @default.
- NCIT_C120223 subClassOf NCIT_C3420 @default.
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- NCIT_C120223 subClassOf NCIT_C36541 @default.
- NCIT_C120223 subClassOf NCIT_C3910 @default.
- NCIT_C120223 subClassOf NCIT_C97926 @default.