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- NCIT_C101071 IAO_0000115 "A fusion gene that results from a chromosomal rearrangement either t(3;3)(q21;q26) or inv(3)(q21q26) which fuses the promoter sequences from the RPN1 gene on either the 5' or 3' side of the coding sequence of the MECOM gene. This rearrangement is associated with overexpression of the MDS1 and EVI1 complex locus protein EVI1 and 3q21q26 syndrome-related leukemias." @default.
- NCIT_C101071 NCIT_NHC0 "C101071" @default.
- NCIT_C101071 NCIT_P106 "Gene or Genome" @default.
- NCIT_C101071 NCIT_P108 "RPN1/MECOM Fusion Gene" @default.
- NCIT_C101071 NCIT_P200 "Fusion_Gene" @default.
- NCIT_C101071 NCIT_P204 "Gene_Involved_In_Pathogenesis_Of_Disease some 'Acute Myeloid Leukemia with inv(3) (q21.3;q26.2) or t(3;3) (q21.3;q26.2); GATA2, MECOM'" @default.
- NCIT_C101071 NCIT_P310 "Retired_Concept" @default.
- NCIT_C101071 NCIT_P98 "Wed Nov 09 08:34:48 EST 2016 - This term is an inaccurate representation of the genetic aberration that is associated with acute myeloid leukemia." @default.
- NCIT_C101071 normalizedInformationContent "100" @default.
- NCIT_C101071 referenceCount "1" @default.
- NCIT_C101071 hasExactSynonym "RPN1-EVI1 Fusion Gene" @default.
- NCIT_C101071 hasExactSynonym "RPN1-MECOM Fusion Gene" @default.
- NCIT_C101071 hasExactSynonym "RPN1/MECOM Fusion Gene" @default.
- NCIT_C101071 type Class @default.
- NCIT_C101071 isDefinedBy ncit.owl @default.
- NCIT_C101071 label "RPN1/MECOM Fusion Gene" @default.
- NCIT_C101071 subClassOf NCIT_C101071 @default.
- NCIT_C101071 subClassOf NCIT_C131742 @default.
- NCIT_C101071 subClassOf NCIT_C28428 @default.
- NCIT_C101071 deprecated "true" @default.