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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/46A733112C18FC7BE3C52D06B9571C0052BC3EB42B9185BC0A52CAEFC34B74F94ADA6A43C7C1FC59AAA45656B13E060A>
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http://purl.uniprot.org/SHA-384/46A733112C18FC7BE3C52D06B9571C0052BC3EB42B9185BC0A52CAEFC34B74F94ADA6A43C7C1FC59AAA45656B13E060A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/46A733112C18FC7BE3C52D06B9571C0052BC3EB42B9185BC0A52CAEFC34B74F94ADA6A43C7C1FC59AAA45656B13E060A
http://www.w3.org/2000/01/rdf-schema#comment
"This case is important not only because of the distinct phenotypic abnormality seen with specific CF mutations but also because of the associated genotype."
xsd:string
http://purl.uniprot.org/uniprot/#_6D7D207E0A4F82145FC764BABDDC62A23B9086AE49E08391D112FB3C67FE56AA24F59FA310EBD5B1B6D5378EADDBE0A2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/46A733112C18FC7BE3C52D06B9571C0052BC3EB42B9185BC0A52CAEFC34B74F94ADA6A43C7C1FC59AAA45656B13E060A
http://purl.uniprot.org/uniprot/A0A088T1A1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/46A733112C18FC7BE3C52D06B9571C0052BC3EB42B9185BC0A52CAEFC34B74F94ADA6A43C7C1FC59AAA45656B13E060A
http://purl.uniprot.org/uniprot/#_A0A088T1A1-mappedCitation-18778819
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/46A733112C18FC7BE3C52D06B9571C0052BC3EB42B9185BC0A52CAEFC34B74F94ADA6A43C7C1FC59AAA45656B13E060A