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DESCRIBE <http://purl.uniprot.org/SHA-384/029324702E755C16EA373D3DB6A452367194FD8E2B5464E40028EF180BA2D4781E440B8A7422F650909F1424811139F4>
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http://purl.uniprot.org/SHA-384/029324702E755C16EA373D3DB6A452367194FD8E2B5464E40028EF180BA2D4781E440B8A7422F650909F1424811139F4
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/029324702E755C16EA373D3DB6A452367194FD8E2B5464E40028EF180BA2D4781E440B8A7422F650909F1424811139F4
http://www.w3.org/2000/01/rdf-schema#comment
"Whole Exome Sequencing Reveals Novel and Recurrent Disease-Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital Cataract."
xsd:string
http://purl.uniprot.org/uniprot/#_18D7E4DAEADCBE4285803D10CF89D43FB5D920C58DA9AA4855C2380E881445E9DDD484C20496EE3109DD40549F0B0976
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/029324702E755C16EA373D3DB6A452367194FD8E2B5464E40028EF180BA2D4781E440B8A7422F650909F1424811139F4
http://purl.uniprot.org/uniprot/A0A097IW74
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/029324702E755C16EA373D3DB6A452367194FD8E2B5464E40028EF180BA2D4781E440B8A7422F650909F1424811139F4
http://purl.uniprot.org/uniprot/#_A0A097IW74-mappedCitation-32384692
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/029324702E755C16EA373D3DB6A452367194FD8E2B5464E40028EF180BA2D4781E440B8A7422F650909F1424811139F4