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DESCRIBE <http://purl.uniprot.org/SHA-384/F6A1C14E3697EB4D095612BC5E32DEA643B89B979E034585924495B4CF53219D6604DD799D44AB5FD5E88C79D881A972>
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http://purl.uniprot.org/SHA-384/F6A1C14E3697EB4D095612BC5E32DEA643B89B979E034585924495B4CF53219D6604DD799D44AB5FD5E88C79D881A972
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F6A1C14E3697EB4D095612BC5E32DEA643B89B979E034585924495B4CF53219D6604DD799D44AB5FD5E88C79D881A972
http://www.w3.org/2000/01/rdf-schema#comment
"CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis."
xsd:string
http://purl.uniprot.org/uniprot/#_E465D84C07E63739355F2F8837A2E387523673950F8BEFE6B12F364EF0E6D95FA556A29C14E3153D8C18607A18174260
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F6A1C14E3697EB4D095612BC5E32DEA643B89B979E034585924495B4CF53219D6604DD799D44AB5FD5E88C79D881A972
http://purl.uniprot.org/uniprot/B3KN48
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F6A1C14E3697EB4D095612BC5E32DEA643B89B979E034585924495B4CF53219D6604DD799D44AB5FD5E88C79D881A972
http://purl.uniprot.org/uniprot/#_B3KN48-mappedCitation-36862503
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F6A1C14E3697EB4D095612BC5E32DEA643B89B979E034585924495B4CF53219D6604DD799D44AB5FD5E88C79D881A972