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DESCRIBE <http://purl.uniprot.org/SHA-384/66E5323501BD613AF8F7DEDF66FCFB71487A6F37521FD224CE3B110BE855A1CD64F8ABA35575741864BBBDC60BB65F09>
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http://purl.uniprot.org/SHA-384/66E5323501BD613AF8F7DEDF66FCFB71487A6F37521FD224CE3B110BE855A1CD64F8ABA35575741864BBBDC60BB65F09
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/66E5323501BD613AF8F7DEDF66FCFB71487A6F37521FD224CE3B110BE855A1CD64F8ABA35575741864BBBDC60BB65F09
http://www.w3.org/2000/01/rdf-schema#comment
"Defective transport at the lysosomal membrane caused by an absence of functional CLN3 is the primary biochemical defect that results in Batten disease."
xsd:string
http://purl.uniprot.org/uniprot/#_5736F84108645FCCDABF7BFB07DD12F319713C68E9E2D1155EE6BC36767F91E9CD27BD3FEBBA190FC846502445014F3B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/66E5323501BD613AF8F7DEDF66FCFB71487A6F37521FD224CE3B110BE855A1CD64F8ABA35575741864BBBDC60BB65F09
http://purl.uniprot.org/uniprot/O95091
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/66E5323501BD613AF8F7DEDF66FCFB71487A6F37521FD224CE3B110BE855A1CD64F8ABA35575741864BBBDC60BB65F09
http://purl.uniprot.org/uniprot/#_O95091-mappedCitation-14660799
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/66E5323501BD613AF8F7DEDF66FCFB71487A6F37521FD224CE3B110BE855A1CD64F8ABA35575741864BBBDC60BB65F09