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- NCIT_C170892 IAO_0000115 "A cytogenetic abnormality that refers to the translocation of the short arm (p21-22) of chromosome 7 and the long arm (q13-15) of chromosome 12. It results in the formation of ACTB/GLI1 fusion gene." @default.
- NCIT_C170892 NCIT_NHC0 "C170892" @default.
- NCIT_C170892 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C170892 NCIT_P108 "t(7;12)(p21-22;q13-15)" @default.
- NCIT_C170892 NCIT_P208 "CL358501" @default.
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- NCIT_C170892 NCIT_R173 NCIT_C14134 @default.
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- NCIT_C170892 NCIT_R177 NCIT_C24432 @default.
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- NCIT_C170892 NCIT_R177 NCIT_C54362 @default.
- NCIT_C170892 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C170892 referenceCount "2" @default.
- NCIT_C170892 hasExactSynonym "t(7;12)(p21-22;q13-15)" @default.
- NCIT_C170892 hasExactSynonym "t(7;12)(p22;q13)" @default.
- NCIT_C170892 type Class @default.
- NCIT_C170892 isDefinedBy ncit.owl @default.
- NCIT_C170892 label "t(7;12)(p21-22;q13-15)" @default.
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- NCIT_C170892 subClassOf NCIT_C186867 @default.
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- NCIT_C170892 subClassOf NCIT_C97926 @default.