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http://purl.uniprot.org/SHA-384/59B411D5A1AB0FFD7D6EFAA6E06DD2DBBD76EA7E66FA2AE5173C2A1C7181C55CB9A34DFA5F911A24753DDE68F08D442Dhttp://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/59B411D5A1AB0FFD7D6EFAA6E06DD2DBBD76EA7E66FA2AE5173C2A1C7181C55CB9A34DFA5F911A24753DDE68F08D442Dhttp://www.w3.org/2000/01/rdf-schema#comment"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; Observational study of genotype prevalence. (HuGE Navigator)"xsd:string
http://purl.uniprot.org/uniprot/#_B14FCA8F60FD08734335B5D7838BC79F331F625683083C2AEFB3A5D9D0927AC80A54B2BD86DCBE566FBDE618DA4E6017http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/59B411D5A1AB0FFD7D6EFAA6E06DD2DBBD76EA7E66FA2AE5173C2A1C7181C55CB9A34DFA5F911A24753DDE68F08D442D
http://purl.uniprot.org/uniprot/A0A3B3IRW4http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/59B411D5A1AB0FFD7D6EFAA6E06DD2DBBD76EA7E66FA2AE5173C2A1C7181C55CB9A34DFA5F911A24753DDE68F08D442D
http://purl.uniprot.org/uniprot/#_A0A3B3IRW4-mappedCitation-17356515http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/59B411D5A1AB0FFD7D6EFAA6E06DD2DBBD76EA7E66FA2AE5173C2A1C7181C55CB9A34DFA5F911A24753DDE68F08D442D