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- NCIT_C13395 IAO_0000115 "A cytogenetic abnormality that involves a translocation between 8q22 and 21q22. It is associated with the development of acute myeloid leukemia with RUNX1-RUNX1T1 fusion protein expression." @default.
- NCIT_C13395 NCIT_NHC0 "C13395" @default.
- NCIT_C13395 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C13395 NCIT_P107 "t(8;21)(q22;q22)" @default.
- NCIT_C13395 NCIT_P108 "t(8;21)(q22;q22)" @default.
- NCIT_C13395 NCIT_P207 "C1515794" @default.
- NCIT_C13395 NCIT_P322 "CTRP" @default.
- NCIT_C13395 NCIT_P366 "t_8_21_q22_q22" @default.
- NCIT_C13395 NCIT_R173 NCIT_C12219 @default.
- NCIT_C13395 NCIT_R173 NCIT_C13202 @default.
- NCIT_C13395 NCIT_R173 NCIT_C13203 @default.
- NCIT_C13395 NCIT_R173 NCIT_C13217 @default.
- NCIT_C13395 NCIT_R173 NCIT_C13224 @default.
- NCIT_C13395 NCIT_R173 NCIT_C13404 @default.
- NCIT_C13395 NCIT_R173 NCIT_C14134 @default.
- NCIT_C13395 NCIT_R173 NCIT_C21599 @default.
- NCIT_C13395 NCIT_R177 NCIT_C16612 @default.
- NCIT_C13395 NCIT_R177 NCIT_C18579 @default.
- NCIT_C13395 NCIT_R177 NCIT_C20420 @default.
- NCIT_C13395 NCIT_R177 NCIT_C28510 @default.
- NCIT_C13395 NCIT_R177 NCIT_C28570 @default.
- NCIT_C13395 NCIT_R177 NCIT_C54362 @default.
- NCIT_C13395 NCIT_R177 NCIT_C99294 @default.
- NCIT_C13395 normalizedInformationContent "84.132738204908478" @default.
- NCIT_C13395 referenceCount "11" @default.
- NCIT_C13395 hasExactSynonym "Eight-Twenty-One" @default.
- NCIT_C13395 hasExactSynonym "t(8;21)(q21.3;q22)" @default.
- NCIT_C13395 hasExactSynonym "t(8;21)(q22; q22.1)" @default.
- NCIT_C13395 hasExactSynonym "t(8;21)(q22;q22)" @default.
- NCIT_C13395 inSubset NCIT_C116977 @default.
- NCIT_C13395 inSubset NCIT_C142799 @default.
- NCIT_C13395 inSubset NCIT_C142800 @default.
- NCIT_C13395 type Class @default.
- NCIT_C13395 isDefinedBy ncit.owl @default.
- NCIT_C13395 label "t(8;21)(q22;q22)" @default.
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- NCIT_C13395 subClassOf NCIT_C186972 @default.
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- NCIT_C13395 subClassOf NCIT_C2950 @default.
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- NCIT_C13395 subClassOf NCIT_C97926 @default.