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- NCIT_C99694 IAO_0000115 "A fusion gene that results from a chromosomal translocation t(6;8)(q27;p11) that fuses intron 8 of the FGFR1 gene with intron 6, 7 or 8 of the FGFR1OP gene. This translocation is associated with 8p11 myeloproliferative disorder." @default.
- NCIT_C99694 NCIT_A13 NCIT_C19929 @default.
- NCIT_C99694 NCIT_A13 NCIT_C24401 @default.
- NCIT_C99694 NCIT_NHC0 "C99694" @default.
- NCIT_C99694 NCIT_P106 "Gene or Genome" @default.
- NCIT_C99694 NCIT_P107 "FGFR1/FGFR1OP Fusion Gene" @default.
- NCIT_C99694 NCIT_P108 "FGFR1/FGFR1OP Fusion Gene" @default.
- NCIT_C99694 NCIT_P207 "C3274866" @default.
- NCIT_C99694 NCIT_P322 "CTRP" @default.
- NCIT_C99694 normalizedInformationContent "100" @default.
- NCIT_C99694 referenceCount "1" @default.
- NCIT_C99694 hasExactSynonym "FGFR1-FGFR1OP Fusion Gene" @default.
- NCIT_C99694 hasExactSynonym "FGFR1-FOP Fusion Gene" @default.
- NCIT_C99694 hasExactSynonym "FGFR1/FGFR1OP Fusion Gene" @default.
- NCIT_C99694 hasExactSynonym "FGFR1/FOP Fusion Gene" @default.
- NCIT_C99694 hasExactSynonym "FGFR1::CEP43 Fusion Gene" @default.
- NCIT_C99694 hasExactSynonym "FGFR1::FGFR1OP Fusion Gene" @default.
- NCIT_C99694 inSubset NCIT_C116977 @default.
- NCIT_C99694 inSubset NCIT_C142799 @default.
- NCIT_C99694 inSubset NCIT_C142800 @default.
- NCIT_C99694 type Class @default.
- NCIT_C99694 isDefinedBy ncit.owl @default.
- NCIT_C99694 label "FGFR1/FGFR1OP Fusion Gene" @default.
- NCIT_C99694 subClassOf NCIT_C16612 @default.
- NCIT_C99694 subClassOf NCIT_C28510 @default.
- NCIT_C99694 subClassOf NCIT_C99694 @default.