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- NCIT_C155906 IAO_0000115 "A cytogenetic abnormality that refers to deletion of chromosome bands 13-14 on the short arm of chromosome 3." @default.
- NCIT_C155906 NCIT_NHC0 "C155906" @default.
- NCIT_C155906 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C155906 NCIT_P108 "del(3p13-14)" @default.
- NCIT_C155906 NCIT_P208 "CL562765" @default.
- NCIT_C155906 NCIT_R173 NCIT_C12219 @default.
- NCIT_C155906 NCIT_R173 NCIT_C13202 @default.
- NCIT_C155906 NCIT_R173 NCIT_C13203 @default.
- NCIT_C155906 NCIT_R173 NCIT_C13219 @default.
- NCIT_C155906 NCIT_R173 NCIT_C13404 @default.
- NCIT_C155906 NCIT_R173 NCIT_C14134 @default.
- NCIT_C155906 NCIT_R173 NCIT_C21599 @default.
- NCIT_C155906 normalizedInformationContent "100" @default.
- NCIT_C155906 referenceCount "1" @default.
- NCIT_C155906 hasExactSynonym "del(3)(p13;p14)" @default.
- NCIT_C155906 hasExactSynonym "del(3p13-14)" @default.
- NCIT_C155906 type Class @default.
- NCIT_C155906 isDefinedBy ncit.owl @default.
- NCIT_C155906 label "del(3p13-14)" @default.
- NCIT_C155906 subClassOf B1f4bc7ace3769f4c3a84127b2008133e @default.
- NCIT_C155906 subClassOf Bb2941a8857ac0d4372ab2ff16289aaac @default.
- NCIT_C155906 subClassOf NCIT_C155906 @default.
- NCIT_C155906 subClassOf NCIT_C2950 @default.
- NCIT_C155906 subClassOf NCIT_C36541 @default.
- NCIT_C155906 subClassOf NCIT_C3910 @default.
- NCIT_C155906 subClassOf NCIT_C9484 @default.