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DESCRIBE <http://purl.uniprot.org/SHA-384/40F95A3C892B1C8AE1B0F11EB2805A920051D7C5F387F3141A4E7326C04D73B5769BC52C52A4760645A85F37E7D2FF07>
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http://purl.uniprot.org/SHA-384/40F95A3C892B1C8AE1B0F11EB2805A920051D7C5F387F3141A4E7326C04D73B5769BC52C52A4760645A85F37E7D2FF07
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/40F95A3C892B1C8AE1B0F11EB2805A920051D7C5F387F3141A4E7326C04D73B5769BC52C52A4760645A85F37E7D2FF07
http://www.w3.org/2000/01/rdf-schema#comment
"The KIND1 mutation c.67insC represents the most common recurrent pathogenic gene mutation in patients with KS."
xsd:string
http://purl.uniprot.org/uniprot/#_45FC4F545D34D80384D425E3A2268CD17596DA31ED08F3C39FF016A1FC9B71F6AAFE8F1CF6CA2CA1927A28E528A0CE3D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/40F95A3C892B1C8AE1B0F11EB2805A920051D7C5F387F3141A4E7326C04D73B5769BC52C52A4760645A85F37E7D2FF07
http://purl.uniprot.org/uniprot/Q9BQL6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/40F95A3C892B1C8AE1B0F11EB2805A920051D7C5F387F3141A4E7326C04D73B5769BC52C52A4760645A85F37E7D2FF07
http://purl.uniprot.org/uniprot/#_Q9BQL6-mappedCitation-17916195
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/40F95A3C892B1C8AE1B0F11EB2805A920051D7C5F387F3141A4E7326C04D73B5769BC52C52A4760645A85F37E7D2FF07