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- NCIT_C185241 IAO_0000115 "A chromosomal anomaly characterized by the partial duplication of the short arm of chromosome 2. The phenotype is highly variable but principally characterized by growth failure, global developmental delay, facial dysmorphism and ocular anomalies." @default.
- NCIT_C185241 NCIT_NHC0 "C185241" @default.
- NCIT_C185241 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C185241 NCIT_P108 "Distal Trisomy 2p" @default.
- NCIT_C185241 NCIT_P208 "CL1773610" @default.
- NCIT_C185241 NCIT_P322 "Cellosaurus" @default.
- NCIT_C185241 NCIT_R173 NCIT_C12219 @default.
- NCIT_C185241 NCIT_R173 NCIT_C13202 @default.
- NCIT_C185241 NCIT_R173 NCIT_C13203 @default.
- NCIT_C185241 NCIT_R173 NCIT_C13215 @default.
- NCIT_C185241 NCIT_R173 NCIT_C13404 @default.
- NCIT_C185241 NCIT_R173 NCIT_C14134 @default.
- NCIT_C185241 NCIT_R173 NCIT_C21599 @default.
- NCIT_C185241 normalizedInformationContent "100" @default.
- NCIT_C185241 referenceCount "1" @default.
- NCIT_C185241 hasExactSynonym "Distal Trisomy 2p" @default.
- NCIT_C185241 inSubset NCIT_C165258 @default.
- NCIT_C185241 inSubset NCIT_C192842 @default.
- NCIT_C185241 type Class @default.
- NCIT_C185241 isDefinedBy ncit.owl @default.
- NCIT_C185241 label "Distal Trisomy 2p" @default.
- NCIT_C185241 subClassOf NCIT_C185241 @default.
- NCIT_C185241 subClassOf NCIT_C2873 @default.
- NCIT_C185241 subClassOf NCIT_C2950 @default.
- NCIT_C185241 subClassOf NCIT_C3421 @default.
- NCIT_C185241 subClassOf NCIT_C36331 @default.
- NCIT_C185241 subClassOf NCIT_C36438 @default.
- NCIT_C185241 subClassOf NCIT_C36439 @default.
- NCIT_C185241 subClassOf NCIT_C3910 @default.
- NCIT_C185241 subClassOf NCIT_C6825 @default.