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DESCRIBE <http://purl.uniprot.org/SHA-384/E10B4D8B473ADA90E8D3B0297EE658F47A36476B516161F4125F7F64EA8531C8351F23A2E71D2A3D9E0CA9BEFDBFE243>
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http://purl.uniprot.org/SHA-384/E10B4D8B473ADA90E8D3B0297EE658F47A36476B516161F4125F7F64EA8531C8351F23A2E71D2A3D9E0CA9BEFDBFE243
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E10B4D8B473ADA90E8D3B0297EE658F47A36476B516161F4125F7F64EA8531C8351F23A2E71D2A3D9E0CA9BEFDBFE243
http://www.w3.org/2000/01/rdf-schema#comment
"The reduction in movement of WT SLC4A11 protein to the cell surface caused by Fuchs endothelial corneal dystrophy SLC4A11 helps to explain the dominant inheritance of this disorder."
xsd:string
http://purl.uniprot.org/uniprot/#_EF318F88277D38BAD8A05CDB5DC2F475596537309075D157110F9531D5BD2CC2AB7475314AE1D9C61E6EF481BF90C3A1
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E10B4D8B473ADA90E8D3B0297EE658F47A36476B516161F4125F7F64EA8531C8351F23A2E71D2A3D9E0CA9BEFDBFE243
http://purl.uniprot.org/uniprot/V9GYK6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E10B4D8B473ADA90E8D3B0297EE658F47A36476B516161F4125F7F64EA8531C8351F23A2E71D2A3D9E0CA9BEFDBFE243
http://purl.uniprot.org/uniprot/#_V9GYK6-mappedCitation-22072594
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E10B4D8B473ADA90E8D3B0297EE658F47A36476B516161F4125F7F64EA8531C8351F23A2E71D2A3D9E0CA9BEFDBFE243