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- NCIT_C36407 IAO_0000115 "A cytogenetic abnormality that refers to a paracentric inversion involving breakpoints on the long (q23.1 and q26.2) of chromosome 3. It is associated with acute myeloid leukemia." @default.
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- NCIT_C36407 NCIT_P106 "Cell or Molecular Dysfunction" @default.
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- NCIT_C36407 NCIT_P207 "C1515666" @default.
- NCIT_C36407 NCIT_P322 "CTRP" @default.
- NCIT_C36407 NCIT_P322 "PCDC" @default.
- NCIT_C36407 NCIT_P366 "inv_3_q21q26_2" @default.
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- NCIT_C36407 NCIT_R177 NCIT_C97552 @default.
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- NCIT_C36407 hasExactSynonym "inv(3)(q21.3;q26.2)" @default.
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- NCIT_C36407 hasExactSynonym "inv(3)(q21;q26.2)" @default.
- NCIT_C36407 hasExactSynonym "inv(3)(q21q26.2)" @default.
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- NCIT_C36407 type Class @default.
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