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DESCRIBE <http://purl.uniprot.org/SHA-384/A17B6C57E2C34F637228903D28E96D0AA81AA4439F74184C5AD39BFA18FF678B805BEEBAD8D95AAD9CB9BF1F3A398D2A>
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http://purl.uniprot.org/SHA-384/A17B6C57E2C34F637228903D28E96D0AA81AA4439F74184C5AD39BFA18FF678B805BEEBAD8D95AAD9CB9BF1F3A398D2A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A17B6C57E2C34F637228903D28E96D0AA81AA4439F74184C5AD39BFA18FF678B805BEEBAD8D95AAD9CB9BF1F3A398D2A
http://www.w3.org/2000/01/rdf-schema#comment
"Protein C deficiency is the major inherited risk factor of VTE. The most common PROC mutation identified in this study was heterozygous c.565C > T missense mutation."
xsd:string
http://purl.uniprot.org/uniprot/#_F77AD6137872B527F0C7A43F080F9F57963D4216AC54872F26C0CCCF9C4D02063B58071C36405AEB200CBC7B76DB81B2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A17B6C57E2C34F637228903D28E96D0AA81AA4439F74184C5AD39BFA18FF678B805BEEBAD8D95AAD9CB9BF1F3A398D2A
http://purl.uniprot.org/uniprot/P04070
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A17B6C57E2C34F637228903D28E96D0AA81AA4439F74184C5AD39BFA18FF678B805BEEBAD8D95AAD9CB9BF1F3A398D2A
http://purl.uniprot.org/uniprot/#_P04070-mappedCitation-22944127
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A17B6C57E2C34F637228903D28E96D0AA81AA4439F74184C5AD39BFA18FF678B805BEEBAD8D95AAD9CB9BF1F3A398D2A