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DESCRIBE <http://purl.uniprot.org/SHA-384/7CC4C8E3D1D24DED784D2E0B9BBB1D61947342791D4DB5EE7198B0E8676C426324095B58B2BE97330D577D07B03A11EF>
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http://purl.uniprot.org/SHA-384/7CC4C8E3D1D24DED784D2E0B9BBB1D61947342791D4DB5EE7198B0E8676C426324095B58B2BE97330D577D07B03A11EF
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7CC4C8E3D1D24DED784D2E0B9BBB1D61947342791D4DB5EE7198B0E8676C426324095B58B2BE97330D577D07B03A11EF
http://www.w3.org/2000/01/rdf-schema#comment
"Thirty-two percent (16/50) of patients were found to be positive for mutations including mutations among RET (n=4) VHL (n=6) SDHB (n=3) and SDHD (n=3) genes."
xsd:string
http://purl.uniprot.org/uniprot/#_F25787E007A4401D52DF21E3121EA9BA20E1075F4FEBF096476C4024A775CAA4ED37C99B4D9EC67A8328B8A9C926B6AD
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7CC4C8E3D1D24DED784D2E0B9BBB1D61947342791D4DB5EE7198B0E8676C426324095B58B2BE97330D577D07B03A11EF
http://purl.uniprot.org/uniprot/G3V173
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7CC4C8E3D1D24DED784D2E0B9BBB1D61947342791D4DB5EE7198B0E8676C426324095B58B2BE97330D577D07B03A11EF
http://purl.uniprot.org/uniprot/#_G3V173-mappedCitation-24977658
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7CC4C8E3D1D24DED784D2E0B9BBB1D61947342791D4DB5EE7198B0E8676C426324095B58B2BE97330D577D07B03A11EF