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- NCIT_C155904 IAO_0000115 "A cytogenetic abnormality that refers to deletion of chromosome bands 21-22 on the short arm of chromosome 3." @default.
- NCIT_C155904 NCIT_NHC0 "C155904" @default.
- NCIT_C155904 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C155904 NCIT_P108 "del(3p21-22)" @default.
- NCIT_C155904 NCIT_P208 "CL562771" @default.
- NCIT_C155904 NCIT_R173 NCIT_C12219 @default.
- NCIT_C155904 NCIT_R173 NCIT_C13202 @default.
- NCIT_C155904 NCIT_R173 NCIT_C13203 @default.
- NCIT_C155904 NCIT_R173 NCIT_C13219 @default.
- NCIT_C155904 NCIT_R173 NCIT_C13404 @default.
- NCIT_C155904 NCIT_R173 NCIT_C14134 @default.
- NCIT_C155904 NCIT_R173 NCIT_C21599 @default.
- NCIT_C155904 normalizedInformationContent "100" @default.
- NCIT_C155904 referenceCount "1" @default.
- NCIT_C155904 hasExactSynonym "del(3)(p21;p22)" @default.
- NCIT_C155904 hasExactSynonym "del(3p21-22)" @default.
- NCIT_C155904 type Class @default.
- NCIT_C155904 isDefinedBy ncit.owl @default.
- NCIT_C155904 label "del(3p21-22)" @default.
- NCIT_C155904 subClassOf B291bff221d496668d71bacee54c36c69 @default.
- NCIT_C155904 subClassOf Baa1db03ccc88c558594b502b6b4bf3d0 @default.
- NCIT_C155904 subClassOf NCIT_C155904 @default.
- NCIT_C155904 subClassOf NCIT_C2950 @default.
- NCIT_C155904 subClassOf NCIT_C36541 @default.
- NCIT_C155904 subClassOf NCIT_C3910 @default.
- NCIT_C155904 subClassOf NCIT_C9484 @default.