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DESCRIBE <http://purl.uniprot.org/SHA-384/BCDB398C544F4EBF96D30E59F28FDD07FB2012A43740C088121D4DF7E0801967356EF99078CF071C9CFE5D50C4BAB414>
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http://purl.uniprot.org/SHA-384/BCDB398C544F4EBF96D30E59F28FDD07FB2012A43740C088121D4DF7E0801967356EF99078CF071C9CFE5D50C4BAB414
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/BCDB398C544F4EBF96D30E59F28FDD07FB2012A43740C088121D4DF7E0801967356EF99078CF071C9CFE5D50C4BAB414
http://www.w3.org/2000/01/rdf-schema#comment
"CLDN19 genetic mutation is responsible for familial magnesium deficiency with hypercalciuria and nephrocalcinosis."
xsd:string
http://purl.uniprot.org/uniprot/#_95157E680516ED660517BBCC1AEE1447678D1C291E7D9944E51E20F564A2CF9D054FEB50B1BF2C4E6EE3CFF89DCD73C2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/BCDB398C544F4EBF96D30E59F28FDD07FB2012A43740C088121D4DF7E0801967356EF99078CF071C9CFE5D50C4BAB414
http://purl.uniprot.org/uniprot/Q8N6F1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BCDB398C544F4EBF96D30E59F28FDD07FB2012A43740C088121D4DF7E0801967356EF99078CF071C9CFE5D50C4BAB414
http://purl.uniprot.org/uniprot/#_Q8N6F1-mappedCitation-25410674
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BCDB398C544F4EBF96D30E59F28FDD07FB2012A43740C088121D4DF7E0801967356EF99078CF071C9CFE5D50C4BAB414