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DESCRIBE <http://purl.uniprot.org/SHA-384/9E8E5E5AE098C107B989E3C08DCE88C81457D16375EDCD2E6A5CEDAD3CEB7313F09025AB72245BE90F773AFF8BDC4EE6>
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http://purl.uniprot.org/SHA-384/9E8E5E5AE098C107B989E3C08DCE88C81457D16375EDCD2E6A5CEDAD3CEB7313F09025AB72245BE90F773AFF8BDC4EE6
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9E8E5E5AE098C107B989E3C08DCE88C81457D16375EDCD2E6A5CEDAD3CEB7313F09025AB72245BE90F773AFF8BDC4EE6
http://www.w3.org/2000/01/rdf-schema#comment
"These results confirm that mutations in the SLC4A11 gene cause autosomal recessive corneal endothelial dystrophy."
xsd:string
http://purl.uniprot.org/uniprot/#_8BDC23C9534E9DD4332C60B0169E6F8B8A5A6CEDE004FD6623DD672DDBFFEF7DF76747846F1EC900DBC3E2490511BD36
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9E8E5E5AE098C107B989E3C08DCE88C81457D16375EDCD2E6A5CEDAD3CEB7313F09025AB72245BE90F773AFF8BDC4EE6
http://purl.uniprot.org/uniprot/R9UQ67
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9E8E5E5AE098C107B989E3C08DCE88C81457D16375EDCD2E6A5CEDAD3CEB7313F09025AB72245BE90F773AFF8BDC4EE6
http://purl.uniprot.org/uniprot/#_R9UQ67-mappedCitation-16825429
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9E8E5E5AE098C107B989E3C08DCE88C81457D16375EDCD2E6A5CEDAD3CEB7313F09025AB72245BE90F773AFF8BDC4EE6