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DESCRIBE <http://purl.uniprot.org/SHA-384/176955D7301E5DAA3F7DBA7C403086D424CE60249277865606D73986A50D26167AB5300B23AC5BFBF2B3FE7C58863410>
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http://purl.uniprot.org/SHA-384/176955D7301E5DAA3F7DBA7C403086D424CE60249277865606D73986A50D26167AB5300B23AC5BFBF2B3FE7C58863410
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/176955D7301E5DAA3F7DBA7C403086D424CE60249277865606D73986A50D26167AB5300B23AC5BFBF2B3FE7C58863410
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/#_A3E1A4B3CA4EADEEA51AA200AE74F4B4E240331A9340585081FBFCF4FE3F002A68AEA243331DB0245BE8731E294F2771
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/176955D7301E5DAA3F7DBA7C403086D424CE60249277865606D73986A50D26167AB5300B23AC5BFBF2B3FE7C58863410
http://purl.uniprot.org/uniprot/R9UQ58
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/176955D7301E5DAA3F7DBA7C403086D424CE60249277865606D73986A50D26167AB5300B23AC5BFBF2B3FE7C58863410
http://purl.uniprot.org/uniprot/#_R9UQ58-mappedCitation-16825429
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/176955D7301E5DAA3F7DBA7C403086D424CE60249277865606D73986A50D26167AB5300B23AC5BFBF2B3FE7C58863410