SPARQL
Downloads
Documentation/Help
Skip Header
Results
Your Query
Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/5062AA96656A91A553320909DDF41ED17E75664572E064F3EF154503C4C6E92264FE71434C2D8A37B7C6144D837D1387>
Submit Query
Cancel
RDF/XML
NTriples
Turtle
Show query
Share
Subject
Predicate
Object
http://purl.uniprot.org/SHA-384/5062AA96656A91A553320909DDF41ED17E75664572E064F3EF154503C4C6E92264FE71434C2D8A37B7C6144D837D1387
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5062AA96656A91A553320909DDF41ED17E75664572E064F3EF154503C4C6E92264FE71434C2D8A37B7C6144D837D1387
http://www.w3.org/2000/01/rdf-schema#comment
"findings support CLN5 hypomorphic mutations cause autosomal recessive cerebellar ataxia confirming other reports showing CLN mutations are associated with adult-onset neurodegenerative disorders"
xsd:string
http://purl.uniprot.org/uniprot/#_AD239EF7C8D9C4890CE1583865EB7376825BB2EC66F60AF8EF2F18ACA8396FFC50C84077617863D3D1726E3A7AE9D0B9
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5062AA96656A91A553320909DDF41ED17E75664572E064F3EF154503C4C6E92264FE71434C2D8A37B7C6144D837D1387
http://purl.uniprot.org/uniprot/O75503
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5062AA96656A91A553320909DDF41ED17E75664572E064F3EF154503C4C6E92264FE71434C2D8A37B7C6144D837D1387
http://purl.uniprot.org/uniprot/#_O75503-mappedCitation-25359263
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5062AA96656A91A553320909DDF41ED17E75664572E064F3EF154503C4C6E92264FE71434C2D8A37B7C6144D837D1387