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DESCRIBE <http://purl.uniprot.org/SHA-384/BDBE7F712F27D3737D12916A2391AD19148FD814C73C2BD842FA12457F5A86E8C764279B8148C743F4CFA6D47B63F206>
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http://purl.uniprot.org/SHA-384/BDBE7F712F27D3737D12916A2391AD19148FD814C73C2BD842FA12457F5A86E8C764279B8148C743F4CFA6D47B63F206
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/BDBE7F712F27D3737D12916A2391AD19148FD814C73C2BD842FA12457F5A86E8C764279B8148C743F4CFA6D47B63F206
http://www.w3.org/2000/01/rdf-schema#comment
"Blau syndrome should be considered in the differential diagnosis of childhood uveitis. Genetic analysis of the CARD15/Nod2 gene is helpful in the diagnosis."
xsd:string
http://purl.uniprot.org/uniprot/#_64A0845DDE0D5D0AB275597638A111461E359BB0C969C5562016EB24F12F7BEB59B05A567860B59579BB5B5255C5DFD1
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/BDBE7F712F27D3737D12916A2391AD19148FD814C73C2BD842FA12457F5A86E8C764279B8148C743F4CFA6D47B63F206
http://purl.uniprot.org/uniprot/B5B2Z4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BDBE7F712F27D3737D12916A2391AD19148FD814C73C2BD842FA12457F5A86E8C764279B8148C743F4CFA6D47B63F206
http://purl.uniprot.org/uniprot/#_B5B2Z4-mappedCitation-14522785
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BDBE7F712F27D3737D12916A2391AD19148FD814C73C2BD842FA12457F5A86E8C764279B8148C743F4CFA6D47B63F206