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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/DDEC3E8597B6F22885A3276A2DC97CEF6179C10B248B14A2A13D8771470463092A798CDBA00ACAE1BB1424A247AB734B>
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http://purl.uniprot.org/SHA-384/DDEC3E8597B6F22885A3276A2DC97CEF6179C10B248B14A2A13D8771470463092A798CDBA00ACAE1BB1424A247AB734B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/DDEC3E8597B6F22885A3276A2DC97CEF6179C10B248B14A2A13D8771470463092A798CDBA00ACAE1BB1424A247AB734B
http://www.w3.org/2000/01/rdf-schema#comment
"study provides initial evidence that a common variant in NLGN3 gene may play a role in the etiology of ASDs among affected males in Chinese Han population."
xsd:string
http://purl.uniprot.org/uniprot/#_C4C8460E15CB75557300A0D3CFEE7B5361788A94E5CCBBCA7AB9657C5EF08D9FEAA4B974103D3209F88031BB50206EF0
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/DDEC3E8597B6F22885A3276A2DC97CEF6179C10B248B14A2A13D8771470463092A798CDBA00ACAE1BB1424A247AB734B
http://purl.uniprot.org/uniprot/B7Z3P8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DDEC3E8597B6F22885A3276A2DC97CEF6179C10B248B14A2A13D8771470463092A798CDBA00ACAE1BB1424A247AB734B
http://purl.uniprot.org/uniprot/#_B7Z3P8-mappedCitation-21569590
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DDEC3E8597B6F22885A3276A2DC97CEF6179C10B248B14A2A13D8771470463092A798CDBA00ACAE1BB1424A247AB734B