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- NCIT_C36368 IAO_0000115 "A cytogenetic abnormality that refers to the translocation of the short arm (p22) of chromosome 7 and the long arm (q12) of chromosome 22." @default.
- NCIT_C36368 NCIT_A28 NCIT_C3910 @default.
- NCIT_C36368 NCIT_NHC0 "C36368" @default.
- NCIT_C36368 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C36368 NCIT_P108 "t(7;22)(p22;q12)" @default.
- NCIT_C36368 NCIT_P207 "C1515787" @default.
- NCIT_C36368 NCIT_P322 "CPTAC" @default.
- NCIT_C36368 NCIT_P322 "PCDC" @default.
- NCIT_C36368 NCIT_P366 "t_7_22_p22_q12" @default.
- NCIT_C36368 NCIT_R173 NCIT_C12219 @default.
- NCIT_C36368 NCIT_R173 NCIT_C13202 @default.
- NCIT_C36368 NCIT_R173 NCIT_C13203 @default.
- NCIT_C36368 NCIT_R173 NCIT_C13218 @default.
- NCIT_C36368 NCIT_R173 NCIT_C13223 @default.
- NCIT_C36368 NCIT_R173 NCIT_C13404 @default.
- NCIT_C36368 NCIT_R173 NCIT_C14134 @default.
- NCIT_C36368 NCIT_R173 NCIT_C21599 @default.
- NCIT_C36368 normalizedInformationContent "73.982472314446994" @default.
- NCIT_C36368 referenceCount "51" @default.
- NCIT_C36368 hasExactSynonym "t(7;22)(p22;q12) (Ewing sarcoma)" @default.
- NCIT_C36368 hasExactSynonym "t(7;22)(p22;q12)" @default.
- NCIT_C36368 inSubset NCIT_C156952 @default.
- NCIT_C36368 inSubset NCIT_C156953 @default.
- NCIT_C36368 inSubset NCIT_C159414 @default.
- NCIT_C36368 inSubset NCIT_C174237 @default.
- NCIT_C36368 inSubset NCIT_C174252 @default.
- NCIT_C36368 type Class @default.
- NCIT_C36368 isDefinedBy ncit.owl @default.
- NCIT_C36368 label "t(7;22)(p22;q12)" @default.
- NCIT_C36368 subClassOf B3937a9820277aa36f5b657234751e8b2 @default.
- NCIT_C36368 subClassOf Befee5ececd529f8c9fd8f8a3f8dbbccc @default.
- NCIT_C36368 subClassOf NCIT_C150479 @default.
- NCIT_C36368 subClassOf NCIT_C159455 @default.
- NCIT_C36368 subClassOf NCIT_C2950 @default.
- NCIT_C36368 subClassOf NCIT_C3420 @default.
- NCIT_C36368 subClassOf NCIT_C36368 @default.
- NCIT_C36368 subClassOf NCIT_C36541 @default.
- NCIT_C36368 subClassOf NCIT_C3910 @default.