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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/777DBAA961F7E7BC83FCDC0C68E4DBCDB60A9419EDF6BB9CE3E7B2C49D592D87B5A50047A20C801A174AB0C7B86B0661>
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http://purl.uniprot.org/SHA-384/777DBAA961F7E7BC83FCDC0C68E4DBCDB60A9419EDF6BB9CE3E7B2C49D592D87B5A50047A20C801A174AB0C7B86B0661
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/777DBAA961F7E7BC83FCDC0C68E4DBCDB60A9419EDF6BB9CE3E7B2C49D592D87B5A50047A20C801A174AB0C7B86B0661
http://www.w3.org/2000/01/rdf-schema#comment
"Mutations in the SLC17A5 gene must be considered in two siblings with hypomyelination even in the absence of sialuria."
xsd:string
http://purl.uniprot.org/uniprot/#_F45C587836EBA25AC02FB710E9AEE289D6FE077949887D802319BB9A70AEADBC749660074C88866B2F40A71478DCF50C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/777DBAA961F7E7BC83FCDC0C68E4DBCDB60A9419EDF6BB9CE3E7B2C49D592D87B5A50047A20C801A174AB0C7B86B0661
http://purl.uniprot.org/uniprot/Q9NRA2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/777DBAA961F7E7BC83FCDC0C68E4DBCDB60A9419EDF6BB9CE3E7B2C49D592D87B5A50047A20C801A174AB0C7B86B0661
http://purl.uniprot.org/uniprot/#_Q9NRA2-mappedCitation-19557856
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/777DBAA961F7E7BC83FCDC0C68E4DBCDB60A9419EDF6BB9CE3E7B2C49D592D87B5A50047A20C801A174AB0C7B86B0661