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- NCIT_C157626 IAO_0000115 "A molecular abnormality that results in monoallelic loss of function mutations located within the short arm of chromosome 1 (1p)." @default.
- NCIT_C157626 NCIT_NHC0 "C157626" @default.
- NCIT_C157626 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C157626 NCIT_P108 "Chromosome Arm 1p Loss of Heterozygosity" @default.
- NCIT_C157626 NCIT_P208 "CL937183" @default.
- NCIT_C157626 NCIT_R173 NCIT_C12219 @default.
- NCIT_C157626 NCIT_R173 NCIT_C13202 @default.
- NCIT_C157626 NCIT_R173 NCIT_C13203 @default.
- NCIT_C157626 NCIT_R173 NCIT_C13204 @default.
- NCIT_C157626 NCIT_R173 NCIT_C13404 @default.
- NCIT_C157626 NCIT_R173 NCIT_C14134 @default.
- NCIT_C157626 NCIT_R173 NCIT_C21599 @default.
- NCIT_C157626 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C157626 referenceCount "2" @default.
- NCIT_C157626 hasExactSynonym "1p LOH" @default.
- NCIT_C157626 hasExactSynonym "1p Loss of Heterozygosity" @default.
- NCIT_C157626 hasExactSynonym "Chromosome Arm 1p Loss of Heterozygosity" @default.
- NCIT_C157626 type Class @default.
- NCIT_C157626 isDefinedBy ncit.owl @default.
- NCIT_C157626 label "Chromosome Arm 1p Loss of Heterozygosity" @default.
- NCIT_C157626 subClassOf NCIT_C157626 @default.
- NCIT_C157626 subClassOf NCIT_C18016 @default.
- NCIT_C157626 subClassOf NCIT_C2950 @default.
- NCIT_C157626 subClassOf NCIT_C36386 @default.
- NCIT_C157626 subClassOf NCIT_C36391 @default.
- NCIT_C157626 subClassOf NCIT_C3910 @default.
- NCIT_C157626 subClassOf NCIT_C45576 @default.
- NCIT_C157626 subClassOf NCIT_C97926 @default.