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DESCRIBE <http://purl.uniprot.org/SHA-384/85667FF771AFCB4336DC6A7A6DD03A13F182A19779F42092B3967C526A1B2E1501D1A2BC2D75E85631C693489135D997>
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http://purl.uniprot.org/SHA-384/85667FF771AFCB4336DC6A7A6DD03A13F182A19779F42092B3967C526A1B2E1501D1A2BC2D75E85631C693489135D997
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/85667FF771AFCB4336DC6A7A6DD03A13F182A19779F42092B3967C526A1B2E1501D1A2BC2D75E85631C693489135D997
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); In addition to chromosomal alterations disrupting the NRXN1alpha promoter rare point mutations in the region may also be involved in SZ pathogenesis."
xsd:string
http://purl.uniprot.org/uniprot/#_A15D370EE5475E61F66510B967DAA5D51D3BFEAC62171EAFB022AF2BD190F22919F68CE63C5060C675423B182D975370
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/85667FF771AFCB4336DC6A7A6DD03A13F182A19779F42092B3967C526A1B2E1501D1A2BC2D75E85631C693489135D997
http://purl.uniprot.org/uniprot/Q08AH0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/85667FF771AFCB4336DC6A7A6DD03A13F182A19779F42092B3967C526A1B2E1501D1A2BC2D75E85631C693489135D997
http://purl.uniprot.org/uniprot/#_Q08AH0-mappedCitation-20347009
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/85667FF771AFCB4336DC6A7A6DD03A13F182A19779F42092B3967C526A1B2E1501D1A2BC2D75E85631C693489135D997