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DESCRIBE <http://purl.uniprot.org/SHA-384/6DB97BD12833FB2E70734EB529465046ABCDFBDF8D3F7F1E6C321F1A52DECB1D584B3B8D570A803F81C8326BA30AF11A>
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http://purl.uniprot.org/SHA-384/6DB97BD12833FB2E70734EB529465046ABCDFBDF8D3F7F1E6C321F1A52DECB1D584B3B8D570A803F81C8326BA30AF11A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/6DB97BD12833FB2E70734EB529465046ABCDFBDF8D3F7F1E6C321F1A52DECB1D584B3B8D570A803F81C8326BA30AF11A
http://www.w3.org/2000/01/rdf-schema#comment
"Frequencies of CFTR variants p.R75Q p.I148T 5T-allele and p.E528E were comparable in patients and controls. We identified 103 CFTR variants which represents a 2.7-fold risk increase (p<0.0001)."
xsd:string
http://purl.uniprot.org/uniprot/#_3671BA335DA281D0FDFEF5A50E3A7A9358A4F8D27B42BA51ED026A77FC9631FEF58489910025D8C8CD4393A73A9D2719
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/6DB97BD12833FB2E70734EB529465046ABCDFBDF8D3F7F1E6C321F1A52DECB1D584B3B8D570A803F81C8326BA30AF11A
http://purl.uniprot.org/uniprot/Q7Z5P3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6DB97BD12833FB2E70734EB529465046ABCDFBDF8D3F7F1E6C321F1A52DECB1D584B3B8D570A803F81C8326BA30AF11A
http://purl.uniprot.org/uniprot/#_Q7Z5P3-mappedCitation-22427236
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6DB97BD12833FB2E70734EB529465046ABCDFBDF8D3F7F1E6C321F1A52DECB1D584B3B8D570A803F81C8326BA30AF11A