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DESCRIBE <http://purl.uniprot.org/SHA-384/75FD32AC0C4CEAA68DECF8AA8D4D450A2202F07E43280DE098E36E1EB0E503B6C35B9960400829756530702FE66A3119>
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http://purl.uniprot.org/SHA-384/75FD32AC0C4CEAA68DECF8AA8D4D450A2202F07E43280DE098E36E1EB0E503B6C35B9960400829756530702FE66A3119
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/75FD32AC0C4CEAA68DECF8AA8D4D450A2202F07E43280DE098E36E1EB0E503B6C35B9960400829756530702FE66A3119
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/#_671F64DBFA5724DD2133AC1F7CDA7D62632CDD96D1F03EA5CD75FC268BD73368809EB3111B7693B3FE3F07090D51B4C2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/75FD32AC0C4CEAA68DECF8AA8D4D450A2202F07E43280DE098E36E1EB0E503B6C35B9960400829756530702FE66A3119
http://purl.uniprot.org/uniprot/A0A0S2Z3Y2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/75FD32AC0C4CEAA68DECF8AA8D4D450A2202F07E43280DE098E36E1EB0E503B6C35B9960400829756530702FE66A3119
http://purl.uniprot.org/uniprot/#_A0A0S2Z3Y2-mappedCitation-21460021
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/75FD32AC0C4CEAA68DECF8AA8D4D450A2202F07E43280DE098E36E1EB0E503B6C35B9960400829756530702FE66A3119