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- NCIT_C188023 IAO_0000115 "A cytogenetic abnormality that refers to allelic gain within the chromosomal arm 1p." @default.
- NCIT_C188023 NCIT_NHC0 "C188023" @default.
- NCIT_C188023 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C188023 NCIT_P108 "Gain of Chromosome 1p" @default.
- NCIT_C188023 NCIT_P208 "CL494945" @default.
- NCIT_C188023 NCIT_R173 NCIT_C12219 @default.
- NCIT_C188023 NCIT_R173 NCIT_C13202 @default.
- NCIT_C188023 NCIT_R173 NCIT_C13203 @default.
- NCIT_C188023 NCIT_R173 NCIT_C13204 @default.
- NCIT_C188023 NCIT_R173 NCIT_C13404 @default.
- NCIT_C188023 NCIT_R173 NCIT_C14134 @default.
- NCIT_C188023 NCIT_R173 NCIT_C21599 @default.
- NCIT_C188023 normalizedInformationContent "100" @default.
- NCIT_C188023 referenceCount "1" @default.
- NCIT_C188023 hasExactSynonym "1p Amplification" @default.
- NCIT_C188023 hasExactSynonym "1p Duplication" @default.
- NCIT_C188023 hasExactSynonym "1p Gain" @default.
- NCIT_C188023 hasExactSynonym "Chromosome 1p Amplification" @default.
- NCIT_C188023 hasExactSynonym "Chromosome 1p Duplication" @default.
- NCIT_C188023 hasExactSynonym "Gain of Chromosome 1p" @default.
- NCIT_C188023 hasExactSynonym "dup(1p)" @default.
- NCIT_C188023 type Class @default.
- NCIT_C188023 isDefinedBy ncit.owl @default.
- NCIT_C188023 label "Gain of Chromosome 1p" @default.
- NCIT_C188023 subClassOf NCIT_C188023 @default.
- NCIT_C188023 subClassOf NCIT_C2950 @default.
- NCIT_C188023 subClassOf NCIT_C36386 @default.
- NCIT_C188023 subClassOf NCIT_C36438 @default.
- NCIT_C188023 subClassOf NCIT_C3910 @default.
- NCIT_C188023 subClassOf NCIT_C6825 @default.