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- NCIT_C131505 IAO_0000115 "A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 15q35. It results in the formation of NUP98/JARID1A fusion gene. It is associated with the development of acute myeloid leukemia with t(11;15)(p15;q35); NUP98-JARID1A." @default.
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- NCIT_C131505 NCIT_A24 NCIT_C3910 @default.
- NCIT_C131505 NCIT_NHC0 "C131505" @default.
- NCIT_C131505 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C131505 NCIT_P108 "t(11;15)(p15;q35)" @default.
- NCIT_C131505 NCIT_P208 "CL514689" @default.
- NCIT_C131505 NCIT_P322 "PCDC" @default.
- NCIT_C131505 NCIT_R173 NCIT_C12219 @default.
- NCIT_C131505 NCIT_R173 NCIT_C13202 @default.
- NCIT_C131505 NCIT_R173 NCIT_C13203 @default.
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- NCIT_C131505 NCIT_R173 NCIT_C13210 @default.
- NCIT_C131505 NCIT_R173 NCIT_C13404 @default.
- NCIT_C131505 NCIT_R173 NCIT_C14134 @default.
- NCIT_C131505 NCIT_R173 NCIT_C21599 @default.
- NCIT_C131505 NCIT_R177 NCIT_C105815 @default.
- NCIT_C131505 NCIT_R177 NCIT_C16612 @default.
- NCIT_C131505 NCIT_R177 NCIT_C20744 @default.
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- NCIT_C131505 NCIT_R177 NCIT_C20820 @default.
- NCIT_C131505 NCIT_R177 NCIT_C21281 @default.
- NCIT_C131505 NCIT_R177 NCIT_C21295 @default.
- NCIT_C131505 NCIT_R177 NCIT_C25939 @default.
- NCIT_C131505 NCIT_R177 NCIT_C28510 @default.
- NCIT_C131505 NCIT_R177 NCIT_C28533 @default.
- NCIT_C131505 NCIT_R177 NCIT_C97595 @default.
- NCIT_C131505 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C131505 referenceCount "2" @default.
- NCIT_C131505 hasExactSynonym "t(11;15)(p15;q35)" @default.
- NCIT_C131505 inSubset NCIT_C173233 @default.
- NCIT_C131505 inSubset NCIT_C173236 @default.
- NCIT_C131505 inSubset NCIT_C174019 @default.
- NCIT_C131505 type Class @default.
- NCIT_C131505 isDefinedBy ncit.owl @default.
- NCIT_C131505 label "t(11;15)(p15;q35)" @default.
- NCIT_C131505 subClassOf B38d34cb589a32aa2de0699ddd72f21af @default.
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- NCIT_C131505 subClassOf NCIT_C3910 @default.
- NCIT_C131505 subClassOf NCIT_C97926 @default.