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DESCRIBE <http://purl.uniprot.org/SHA-384/3A9CE9FAA37DB7C13497A478D094425A66FB59B9A4900159FBBC1DA3DE9865654DE32B8AE4D8B708E8B0D8E3ADFAEF68>
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http://purl.uniprot.org/SHA-384/3A9CE9FAA37DB7C13497A478D094425A66FB59B9A4900159FBBC1DA3DE9865654DE32B8AE4D8B708E8B0D8E3ADFAEF68
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/3A9CE9FAA37DB7C13497A478D094425A66FB59B9A4900159FBBC1DA3DE9865654DE32B8AE4D8B708E8B0D8E3ADFAEF68
http://www.w3.org/2000/01/rdf-schema#comment
"IRF-1 gene deletions were not observed in 19 (38%) patients. In our study the frequency of deletions of these three exons was slightly higher than in an Indian population (52%) but lower than in Sweden in Europe (95%)."
xsd:string
http://purl.uniprot.org/uniprot/#_CE472C94CBAFFE8FD918AC4529D25579B0DA77F112643122C44314FF969A401E2B71BD0E2209E99859514B0F1C9DF032
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/3A9CE9FAA37DB7C13497A478D094425A66FB59B9A4900159FBBC1DA3DE9865654DE32B8AE4D8B708E8B0D8E3ADFAEF68
http://purl.uniprot.org/uniprot/Q5FBX3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/3A9CE9FAA37DB7C13497A478D094425A66FB59B9A4900159FBBC1DA3DE9865654DE32B8AE4D8B708E8B0D8E3ADFAEF68
http://purl.uniprot.org/uniprot/#_Q5FBX3-mappedCitation-21790247
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/3A9CE9FAA37DB7C13497A478D094425A66FB59B9A4900159FBBC1DA3DE9865654DE32B8AE4D8B708E8B0D8E3ADFAEF68