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- NCIT_C192089 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the KCNV2 gene, encoding potassium voltage-gated channel subfamily V member 2. It is characterized by photophobia, progressive loss of visual acuity and reduced color discrimination." @default.
- NCIT_C192089 NCIT_NHC0 "C192089" @default.
- NCIT_C192089 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C192089 NCIT_P108 "Retinal Cone Dystrophy 3B" @default.
- NCIT_C192089 NCIT_P207 "C1835897" @default.
- NCIT_C192089 NCIT_P322 "Cellosaurus" @default.
- NCIT_C192089 NCIT_R100 NCIT_C12219 @default.
- NCIT_C192089 NCIT_R100 NCIT_C12343 @default.
- NCIT_C192089 NCIT_R100 NCIT_C12401 @default.
- NCIT_C192089 NCIT_R100 NCIT_C13018 @default.
- NCIT_C192089 NCIT_R100 NCIT_C13019 @default.
- NCIT_C192089 NCIT_R100 NCIT_C32221 @default.
- NCIT_C192089 NCIT_R100 NCIT_C33224 @default.
- NCIT_C192089 NCIT_R100 NCIT_C38626 @default.
- NCIT_C192089 NCIT_R108 NCIT_C3367 @default.
- NCIT_C192089 NCIT_R108 NCIT_C3824 @default.
- NCIT_C192089 NCIT_R108 NCIT_C54062 @default.
- NCIT_C192089 NCIT_R108 NCIT_C7057 @default.
- NCIT_C192089 normalizedInformationContent "100" @default.
- NCIT_C192089 referenceCount "1" @default.
- NCIT_C192089 hasExactSynonym "RCD3B" @default.
- NCIT_C192089 hasExactSynonym "Retinal Cone Dystrophy 3B" @default.
- NCIT_C192089 inSubset NCIT_C165258 @default.
- NCIT_C192089 inSubset NCIT_C192842 @default.
- NCIT_C192089 type Class @default.
- NCIT_C192089 isDefinedBy ncit.owl @default.
- NCIT_C192089 label "Retinal Cone Dystrophy 3B" @default.
- NCIT_C192089 subClassOf NCIT_C192089 @default.
- NCIT_C192089 subClassOf NCIT_C26767 @default.
- NCIT_C192089 subClassOf NCIT_C26875 @default.
- NCIT_C192089 subClassOf NCIT_C27551 @default.
- NCIT_C192089 subClassOf NCIT_C27604 @default.
- NCIT_C192089 subClassOf NCIT_C27610 @default.
- NCIT_C192089 subClassOf NCIT_C2991 @default.
- NCIT_C192089 subClassOf NCIT_C35194 @default.
- NCIT_C192089 subClassOf NCIT_C35625 @default.
- NCIT_C192089 subClassOf NCIT_C53529 @default.
- NCIT_C192089 subClassOf NCIT_C53531 @default.
- NCIT_C192089 subClassOf NCIT_C7057 @default.