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DESCRIBE <http://purl.uniprot.org/SHA-384/18D84CE2FAB4CCB179AB9268D3108294C72BA274CD3A05A5EFB6E811B85D47A06E3E818D5407E93CE07F5670BD3E4FCD>
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http://purl.uniprot.org/SHA-384/18D84CE2FAB4CCB179AB9268D3108294C72BA274CD3A05A5EFB6E811B85D47A06E3E818D5407E93CE07F5670BD3E4FCD
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/18D84CE2FAB4CCB179AB9268D3108294C72BA274CD3A05A5EFB6E811B85D47A06E3E818D5407E93CE07F5670BD3E4FCD
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/#_55B79DB3683B02F329C4ED663A52F67F0BADB38850AFE36C452B1B5C5FE1285036E57FDEC005FF8CAC1032D7072272CC
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/18D84CE2FAB4CCB179AB9268D3108294C72BA274CD3A05A5EFB6E811B85D47A06E3E818D5407E93CE07F5670BD3E4FCD
http://purl.uniprot.org/uniprot/A0A0D9SEM5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/18D84CE2FAB4CCB179AB9268D3108294C72BA274CD3A05A5EFB6E811B85D47A06E3E818D5407E93CE07F5670BD3E4FCD
http://purl.uniprot.org/uniprot/#_A0A0D9SEM5-mappedCitation-28641109
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/18D84CE2FAB4CCB179AB9268D3108294C72BA274CD3A05A5EFB6E811B85D47A06E3E818D5407E93CE07F5670BD3E4FCD