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DESCRIBE <http://purl.uniprot.org/SHA-384/E88E9256C6F43F66EBEDFFC3948ABE84961BF3DE19C26903419599B3A4973B798A85AAC6A81B006FF05A8977D0E90D8A>
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http://purl.uniprot.org/SHA-384/E88E9256C6F43F66EBEDFFC3948ABE84961BF3DE19C26903419599B3A4973B798A85AAC6A81B006FF05A8977D0E90D8A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E88E9256C6F43F66EBEDFFC3948ABE84961BF3DE19C26903419599B3A4973B798A85AAC6A81B006FF05A8977D0E90D8A
http://www.w3.org/2000/01/rdf-schema#comment
"OFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilin"
xsd:string
http://purl.uniprot.org/uniprot/#_E7FF9B9CB6125366F18E7200174CB635711464A17FF5DE3734CC8BE0A8D32C5CAE18332E940546791F6A6033EEC1D1FB
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E88E9256C6F43F66EBEDFFC3948ABE84961BF3DE19C26903419599B3A4973B798A85AAC6A81B006FF05A8977D0E90D8A
http://purl.uniprot.org/uniprot/A8K2T9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E88E9256C6F43F66EBEDFFC3948ABE84961BF3DE19C26903419599B3A4973B798A85AAC6A81B006FF05A8977D0E90D8A
http://purl.uniprot.org/uniprot/#_A8K2T9-mappedCitation-19800048
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E88E9256C6F43F66EBEDFFC3948ABE84961BF3DE19C26903419599B3A4973B798A85AAC6A81B006FF05A8977D0E90D8A