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http://purl.uniprot.org/SHA-384/0BAFDCD5DFDBAF1F2310F8ECA005D344C4CD9F2A15C0EE99B0CE61A1E9D42507C27A2267B984C1B2C2F9F6E65051ED3Dhttp://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/0BAFDCD5DFDBAF1F2310F8ECA005D344C4CD9F2A15C0EE99B0CE61A1E9D42507C27A2267B984C1B2C2F9F6E65051ED3Dhttp://www.w3.org/2000/01/rdf-schema#comment"Observational study of genotype prevalence. (HuGE Navigator); While digenic disease with the SP4 Asn306Ser and the GNB1 intronic variant alleles has not been established neither has it been ruled out. This leaves open the possibility of a cooperative involvement of SP4 and GNB1 in the normal function of the retina."xsd:string
http://purl.uniprot.org/uniprot/#_AF8290BEE15B874B7A1BC246ECE58C1872A2065675E843E779D275D552FC6D405E0BDF8C5ED28B74CB0DCDED7537C7A6http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/0BAFDCD5DFDBAF1F2310F8ECA005D344C4CD9F2A15C0EE99B0CE61A1E9D42507C27A2267B984C1B2C2F9F6E65051ED3D
http://purl.uniprot.org/uniprot/Q02446http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/0BAFDCD5DFDBAF1F2310F8ECA005D344C4CD9F2A15C0EE99B0CE61A1E9D42507C27A2267B984C1B2C2F9F6E65051ED3D
http://purl.uniprot.org/uniprot/#_Q02446-mappedCitation-17356515http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/0BAFDCD5DFDBAF1F2310F8ECA005D344C4CD9F2A15C0EE99B0CE61A1E9D42507C27A2267B984C1B2C2F9F6E65051ED3D