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DESCRIBE <http://purl.uniprot.org/SHA-384/7A179FC4CAA6CDD1E2D821AEC78207620D990EB1BF6CCA3C7F1CC24D39B5A31E5050523869BC919A2FE46311EE45DF4A>
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http://purl.uniprot.org/SHA-384/7A179FC4CAA6CDD1E2D821AEC78207620D990EB1BF6CCA3C7F1CC24D39B5A31E5050523869BC919A2FE46311EE45DF4A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7A179FC4CAA6CDD1E2D821AEC78207620D990EB1BF6CCA3C7F1CC24D39B5A31E5050523869BC919A2FE46311EE45DF4A
http://www.w3.org/2000/01/rdf-schema#comment
"The D47N mutation of Cx50 causes the hereditary nuclear cataract in this family in an autosomal dominant mode of inheritance with incomplete penetrance."
xsd:string
http://purl.uniprot.org/uniprot/#_EB922FA90ACE56F24DDB3572A195BB1EB63776FA694CB7EF409B9222853C76FD5098E7AA90F67D481F11B6EC12B492F6
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7A179FC4CAA6CDD1E2D821AEC78207620D990EB1BF6CCA3C7F1CC24D39B5A31E5050523869BC919A2FE46311EE45DF4A
http://purl.uniprot.org/uniprot/A0A097IW49
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7A179FC4CAA6CDD1E2D821AEC78207620D990EB1BF6CCA3C7F1CC24D39B5A31E5050523869BC919A2FE46311EE45DF4A
http://purl.uniprot.org/uniprot/#_A0A097IW49-mappedCitation-21174522
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7A179FC4CAA6CDD1E2D821AEC78207620D990EB1BF6CCA3C7F1CC24D39B5A31E5050523869BC919A2FE46311EE45DF4A