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DESCRIBE <http://purl.uniprot.org/SHA-384/67229CCA125303D4D14F747B791568890F681F24621C164A6671478C2277A79ABD60E8C8E308ED6AE1807F558845A10B>
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http://purl.uniprot.org/SHA-384/67229CCA125303D4D14F747B791568890F681F24621C164A6671478C2277A79ABD60E8C8E308ED6AE1807F558845A10B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/67229CCA125303D4D14F747B791568890F681F24621C164A6671478C2277A79ABD60E8C8E308ED6AE1807F558845A10B
http://www.w3.org/2000/01/rdf-schema#comment
"The autosomal recessive disorder because of a single mutation in interferon-gamma receptor-1(IFNGR1) at position -56 was found to be associated with susceptibility to leprosy in children of the same family."
xsd:string
http://purl.uniprot.org/uniprot/#_4E906A3EEF383289C039E5252B1A6CEE92A48B8B80C77EEF8EDDC4BC6DDBF97A4DBFD0B55578B5078929D61CAF06835B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/67229CCA125303D4D14F747B791568890F681F24621C164A6671478C2277A79ABD60E8C8E308ED6AE1807F558845A10B
http://purl.uniprot.org/uniprot/E5QBZ2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/67229CCA125303D4D14F747B791568890F681F24621C164A6671478C2277A79ABD60E8C8E308ED6AE1807F558845A10B
http://purl.uniprot.org/uniprot/#_E5QBZ2-mappedCitation-21460021
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/67229CCA125303D4D14F747B791568890F681F24621C164A6671478C2277A79ABD60E8C8E308ED6AE1807F558845A10B