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- NCIT_C105817 IAO_0000115 "A fusion gene that results from a chromosomal translocation t(7;12)(q36;p13) which fuses the first exon of the MNX1 gene with exon 3 of the ETV6 gene. This aberration is associated with infant acute myeloid leukemia." @default.
- NCIT_C105817 NCIT_A13 NCIT_C18312 @default.
- NCIT_C105817 NCIT_A13 NCIT_C97559 @default.
- NCIT_C105817 NCIT_NHC0 "C105817" @default.
- NCIT_C105817 NCIT_P106 "Gene or Genome" @default.
- NCIT_C105817 NCIT_P107 "MNX1/ETV6 Fusion Gene" @default.
- NCIT_C105817 NCIT_P108 "MNX1/ETV6 Fusion Gene" @default.
- NCIT_C105817 NCIT_P207 "C3828997" @default.
- NCIT_C105817 NCIT_P322 "CTRP" @default.
- NCIT_C105817 NCIT_P98 "The presence of this fusion is associated with poor prognosis." @default.
- NCIT_C105817 NCIT_R175 NCIT_C122603 @default.
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- NCIT_C105817 NCIT_R175 NCIT_C9160 @default.
- NCIT_C105817 NCIT_R175 NCIT_C9290 @default.
- NCIT_C105817 NCIT_R175 NCIT_C9300 @default.
- NCIT_C105817 NCIT_R175 NCIT_C9305 @default.
- NCIT_C105817 NCIT_R175 NCIT_C9431 @default.
- NCIT_C105817 normalizedInformationContent "90.826665450122817" @default.
- NCIT_C105817 referenceCount "4" @default.
- NCIT_C105817 hasExactSynonym "HLXB9-ETV6 Fusion Gene" @default.
- NCIT_C105817 hasExactSynonym "HLXB9/ETV6 Fusion Gene" @default.
- NCIT_C105817 hasExactSynonym "MNX1-ETV6 Fusion Gene" @default.
- NCIT_C105817 hasExactSynonym "MNX1/ETV6 Fusion Gene" @default.
- NCIT_C105817 hasExactSynonym "MNX1::ETV6 Fusion Gene" @default.
- NCIT_C105817 inSubset NCIT_C116977 @default.
- NCIT_C105817 inSubset NCIT_C142799 @default.
- NCIT_C105817 inSubset NCIT_C142800 @default.
- NCIT_C105817 type Class @default.
- NCIT_C105817 isDefinedBy ncit.owl @default.
- NCIT_C105817 label "MNX1/ETV6 Fusion Gene" @default.
- NCIT_C105817 subClassOf B2bb87bfd530b8fdbc15be173e13d1f86 @default.
- NCIT_C105817 subClassOf Badea86a82e473e1aec487473338368c0 @default.
- NCIT_C105817 subClassOf NCIT_C105817 @default.
- NCIT_C105817 subClassOf NCIT_C16612 @default.
- NCIT_C105817 subClassOf NCIT_C28510 @default.