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DESCRIBE <http://purl.uniprot.org/SHA-384/AF35EDF2438D0CA5E5CA7CA3FB2AC25C8D25C225D15C79AC4A01FDC5A428D5DABD64C612C68B5605F91D468E673969B3>
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http://purl.uniprot.org/SHA-384/AF35EDF2438D0CA5E5CA7CA3FB2AC25C8D25C225D15C79AC4A01FDC5A428D5DABD64C612C68B5605F91D468E673969B3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/AF35EDF2438D0CA5E5CA7CA3FB2AC25C8D25C225D15C79AC4A01FDC5A428D5DABD64C612C68B5605F91D468E673969B3
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/#_FD0F8F661A055A1E188EAA141B5E93B3A357B4FD3C5103BBC45F7F7EFFB2FC9500D9C3D27667B29EB723CC3554ECE676
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/AF35EDF2438D0CA5E5CA7CA3FB2AC25C8D25C225D15C79AC4A01FDC5A428D5DABD64C612C68B5605F91D468E673969B3
http://purl.uniprot.org/uniprot/Q7Z687
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AF35EDF2438D0CA5E5CA7CA3FB2AC25C8D25C225D15C79AC4A01FDC5A428D5DABD64C612C68B5605F91D468E673969B3
http://purl.uniprot.org/uniprot/#_Q7Z687-mappedCitation-21460021
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AF35EDF2438D0CA5E5CA7CA3FB2AC25C8D25C225D15C79AC4A01FDC5A428D5DABD64C612C68B5605F91D468E673969B3