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DESCRIBE <http://purl.uniprot.org/SHA-384/892D44E0F657BAED294B1865BB4846E2B4AFD57F84E66E6DF0C35156BF0F5B7BA3E7CB7DA760888B986E831D74ED5C8A>
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http://purl.uniprot.org/SHA-384/892D44E0F657BAED294B1865BB4846E2B4AFD57F84E66E6DF0C35156BF0F5B7BA3E7CB7DA760888B986E831D74ED5C8A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/892D44E0F657BAED294B1865BB4846E2B4AFD57F84E66E6DF0C35156BF0F5B7BA3E7CB7DA760888B986E831D74ED5C8A
http://www.w3.org/2000/01/rdf-schema#comment
"Most frequent mutation c.3402delC (p.Ala1135GlnfsX13) among Wilson disease patients in Venezuela has a wide distribution and two old origins"
xsd:string
http://purl.uniprot.org/uniprot/#_7235798BC55DBFD63D36E86B508BDB3CE1C026B62909F7E2B1B2A0727F9FC35BF9A7B2FA411DABDA4E3AF7BBF247C7EA
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/892D44E0F657BAED294B1865BB4846E2B4AFD57F84E66E6DF0C35156BF0F5B7BA3E7CB7DA760888B986E831D74ED5C8A
http://purl.uniprot.org/uniprot/B7ZLR3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/892D44E0F657BAED294B1865BB4846E2B4AFD57F84E66E6DF0C35156BF0F5B7BA3E7CB7DA760888B986E831D74ED5C8A
http://purl.uniprot.org/uniprot/#_B7ZLR3-mappedCitation-25497208
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/892D44E0F657BAED294B1865BB4846E2B4AFD57F84E66E6DF0C35156BF0F5B7BA3E7CB7DA760888B986E831D74ED5C8A