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- NCIT_C168757 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the CNGA3 gene, encoding cyclic nucleotide-gated cation channel subunit alpha-3. It is characterized by achromatopsia." @default.
- NCIT_C168757 NCIT_NHC0 "C168757" @default.
- NCIT_C168757 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C168757 NCIT_P108 "Achromatopsia 2" @default.
- NCIT_C168757 NCIT_P207 "C1857618" @default.
- NCIT_C168757 NCIT_P322 "Cellosaurus" @default.
- NCIT_C168757 NCIT_R176 NCIT_C16612 @default.
- NCIT_C168757 NCIT_R176 NCIT_C200232 @default.
- NCIT_C168757 NCIT_R176 NCIT_C21295 @default.
- NCIT_C168757 NCIT_R176 NCIT_C25869 @default.
- NCIT_C168757 NCIT_R176 NCIT_C25993 @default.
- NCIT_C168757 NCIT_R176 NCIT_C26039 @default.
- NCIT_C168757 NCIT_R176 NCIT_C28533 @default.
- NCIT_C168757 normalizedInformationContent "100" @default.
- NCIT_C168757 referenceCount "1" @default.
- NCIT_C168757 hasExactSynonym "ACHM2" @default.
- NCIT_C168757 hasExactSynonym "Achromatopsia 2" @default.
- NCIT_C168757 inSubset NCIT_C165258 @default.
- NCIT_C168757 inSubset NCIT_C192842 @default.
- NCIT_C168757 type Class @default.
- NCIT_C168757 isDefinedBy ncit.owl @default.
- NCIT_C168757 label "Achromatopsia 2" @default.
- NCIT_C168757 subClassOf B75fa72e610e302547f5d19b3f2d68d64 @default.
- NCIT_C168757 subClassOf Ba6b80873df6e5f67878f9dccafcc2881 @default.
- NCIT_C168757 subClassOf NCIT_C168757 @default.
- NCIT_C168757 subClassOf NCIT_C2991 @default.
- NCIT_C168757 subClassOf NCIT_C4873 @default.
- NCIT_C168757 subClassOf NCIT_C53529 @default.
- NCIT_C168757 subClassOf NCIT_C53543 @default.
- NCIT_C168757 subClassOf NCIT_C53547 @default.
- NCIT_C168757 subClassOf NCIT_C7057 @default.
- NCIT_C168757 subClassOf NCIT_C84528 @default.