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- NCIT_C129079 IAO_0000115 "Human RHO wild-type allele is located in the vicinity of 3q22.1 and is approximately 7 kb in length. This allele, which encodes rhodopsin protein, is involved in photoreceptor cell activity and maintenance. Mutation of the gene is associated with congenital stationary night blindness, retinitis pigmentosa 4, and retinitis punctata albescens." @default.
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- NCIT_C129079 NCIT_P100 "180380" @default.
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- NCIT_C129079 NCIT_P106 "Gene or Genome" @default.
- NCIT_C129079 NCIT_P107 "RHO wt Allele" @default.
- NCIT_C129079 NCIT_P108 "RHO wt Allele" @default.
- NCIT_C129079 NCIT_P208 "CL512326" @default.
- NCIT_C129079 NCIT_P321 "6010" @default.
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- NCIT_C129079 NCIT_R41 NCIT_C14182 @default.
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- NCIT_C129079 NCIT_R41 NCIT_C14262 @default.
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- NCIT_C129079 NCIT_R41 NCIT_C25796 @default.
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- NCIT_C129079 normalizedInformationContent "100" @default.
- NCIT_C129079 referenceCount "1" @default.
- NCIT_C129079 hasExactSynonym "CSNBAD1" @default.
- NCIT_C129079 hasExactSynonym "OPN2" @default.
- NCIT_C129079 hasExactSynonym "Opsin 2, Rod Pigment Gene" @default.
- NCIT_C129079 hasExactSynonym "RHO wt Allele" @default.
- NCIT_C129079 hasExactSynonym "RP4" @default.
- NCIT_C129079 hasExactSynonym "Retinitis Pigmentosa 4, Autosomal Dominant Gene" @default.
- NCIT_C129079 hasExactSynonym "Rhodopsin wt Allele" @default.
- NCIT_C129079 inSubset NCIT_C116977 @default.
- NCIT_C129079 inSubset NCIT_C142799 @default.
- NCIT_C129079 inSubset NCIT_C142800 @default.
- NCIT_C129079 type Class @default.
- NCIT_C129079 isDefinedBy ncit.owl @default.
- NCIT_C129079 label "RHO wt Allele" @default.
- NCIT_C129079 subClassOf NCIT_C129078 @default.
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