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DESCRIBE <http://purl.uniprot.org/SHA-384/B9BBD846B5518B6CED0A72E022B0F5E080DCF1685BC7CFB9A342C579BED8F144D82A348A7B1312E3986244F4FE4E5658>
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http://purl.uniprot.org/SHA-384/B9BBD846B5518B6CED0A72E022B0F5E080DCF1685BC7CFB9A342C579BED8F144D82A348A7B1312E3986244F4FE4E5658
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B9BBD846B5518B6CED0A72E022B0F5E080DCF1685BC7CFB9A342C579BED8F144D82A348A7B1312E3986244F4FE4E5658
http://www.w3.org/2000/01/rdf-schema#comment
"NRXN1 copy number variants (deletions) were associated with increased risk of Tourette syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_02F6E3662009939FA662C2FC3B842E2313162B3DC20D737FFAA0B0753EC08F89BE72922EDDD139B02235982DB69B04B4
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B9BBD846B5518B6CED0A72E022B0F5E080DCF1685BC7CFB9A342C579BED8F144D82A348A7B1312E3986244F4FE4E5658
http://purl.uniprot.org/uniprot/A0A0D9SEQ7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B9BBD846B5518B6CED0A72E022B0F5E080DCF1685BC7CFB9A342C579BED8F144D82A348A7B1312E3986244F4FE4E5658
http://purl.uniprot.org/uniprot/#_A0A0D9SEQ7-mappedCitation-28641109
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B9BBD846B5518B6CED0A72E022B0F5E080DCF1685BC7CFB9A342C579BED8F144D82A348A7B1312E3986244F4FE4E5658