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DESCRIBE <http://purl.uniprot.org/SHA-384/C02E8455980CD3519FEF251A1564914FBC22D38008E08AEB9C790EC830CBDDF55AF82986E03BBC406558D2A5BB0EF33E>
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http://purl.uniprot.org/SHA-384/C02E8455980CD3519FEF251A1564914FBC22D38008E08AEB9C790EC830CBDDF55AF82986E03BBC406558D2A5BB0EF33E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C02E8455980CD3519FEF251A1564914FBC22D38008E08AEB9C790EC830CBDDF55AF82986E03BBC406558D2A5BB0EF33E
http://www.w3.org/2000/01/rdf-schema#comment
"the c.273+11dup change within the WAS gene was observed in patients showing symptoms consistent with the Wiskott-Aldrich syndrome; concluded that the presence of the additional C in the WAS gene is a functionally neutral polymorphism"
xsd:string
http://purl.uniprot.org/uniprot/#_7FAB0614921EB31D8E5545ACCCE7E31043D9DB3AB8FB47013F0729F3498E08831A5A338C3BF86B7C5ACB5767F5648345
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C02E8455980CD3519FEF251A1564914FBC22D38008E08AEB9C790EC830CBDDF55AF82986E03BBC406558D2A5BB0EF33E
http://purl.uniprot.org/uniprot/P42768
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C02E8455980CD3519FEF251A1564914FBC22D38008E08AEB9C790EC830CBDDF55AF82986E03BBC406558D2A5BB0EF33E
http://purl.uniprot.org/uniprot/#_P42768-mappedCitation-21711396
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C02E8455980CD3519FEF251A1564914FBC22D38008E08AEB9C790EC830CBDDF55AF82986E03BBC406558D2A5BB0EF33E