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- NCIT_C99186 IAO_0000115 "A fusion gene that results from a chromosomal translocation t(15;17)(q22;q21) which fuses the first 3 exons of the PML gene with the last 7 exons of the RARA gene. This fusion is associated with acute promyelocytic leukemia. Three transcript variants are possible based on the three breakpoint clusters in the PML gene." @default.
- NCIT_C99186 NCIT_A13 NCIT_C21571 @default.
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- NCIT_C99186 NCIT_NHC0 "C99186" @default.
- NCIT_C99186 NCIT_P102 "M73779" @default.
- NCIT_C99186 NCIT_P106 "Gene or Genome" @default.
- NCIT_C99186 NCIT_P107 "PML/RARA Fusion Gene" @default.
- NCIT_C99186 NCIT_P108 "PML/RARA Fusion Gene" @default.
- NCIT_C99186 NCIT_P207 "C3887967" @default.
- NCIT_C99186 NCIT_P322 "CPTAC" @default.
- NCIT_C99186 NCIT_P322 "CTRP" @default.
- NCIT_C99186 NCIT_P98 "The translocation, well known as t(15;17)(q22;q21) or t(15;17)(q22;q12), should be re-named t(15;17)(q24;q21), since the PML gene is located in the vicinity of 15q24, and the RARA gene is located in the vicinity of 17q21. (Atlas of Genetics and Cytogenetics in Oncology and Haematology)" @default.
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- NCIT_C99186 normalizedInformationContent "84.76342111748103" @default.
- NCIT_C99186 referenceCount "10" @default.
- NCIT_C99186 hasExactSynonym "PML-RAR Alpha Fusion Gene" @default.
- NCIT_C99186 hasExactSynonym "PML-RAR" @default.
- NCIT_C99186 hasExactSynonym "PML-RARA Fusion Gene" @default.
- NCIT_C99186 hasExactSynonym "PML/RARA Fusion Gene" @default.
- NCIT_C99186 hasExactSynonym "PML::RARA Fusion Gene" @default.
- NCIT_C99186 inSubset NCIT_C116977 @default.
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- NCIT_C99186 type Class @default.
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- NCIT_C99186 label "PML/RARA Fusion Gene" @default.
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