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DESCRIBE <http://purl.uniprot.org/SHA-384/3E3513A3A69C590820C097DF2FDFECD4895C789BEA055EE8AE880FCC55B7FA4A26D0DF921377C9E2F9CC3CE48407682D>
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http://purl.uniprot.org/SHA-384/3E3513A3A69C590820C097DF2FDFECD4895C789BEA055EE8AE880FCC55B7FA4A26D0DF921377C9E2F9CC3CE48407682D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/3E3513A3A69C590820C097DF2FDFECD4895C789BEA055EE8AE880FCC55B7FA4A26D0DF921377C9E2F9CC3CE48407682D
http://www.w3.org/2000/01/rdf-schema#comment
"Kidney disease occurs in up to one third of patients with Joubert syndrome most commonly in those with mutations in CEP290 TMEM67 and AHI1."
xsd:string
http://purl.uniprot.org/uniprot/#_85F377F9B9E7B2F70B9F85B4C4FF8347AD50E683AF07458B2D0763DF54AF5FB12E3F164CAED6F279CF2687F03706D298
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/3E3513A3A69C590820C097DF2FDFECD4895C789BEA055EE8AE880FCC55B7FA4A26D0DF921377C9E2F9CC3CE48407682D
http://purl.uniprot.org/uniprot/A0A0S2Z611
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/3E3513A3A69C590820C097DF2FDFECD4895C789BEA055EE8AE880FCC55B7FA4A26D0DF921377C9E2F9CC3CE48407682D
http://purl.uniprot.org/uniprot/#_A0A0S2Z611-mappedCitation-29146704
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/3E3513A3A69C590820C097DF2FDFECD4895C789BEA055EE8AE880FCC55B7FA4A26D0DF921377C9E2F9CC3CE48407682D