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DESCRIBE <http://purl.uniprot.org/SHA-384/5E6F275305B7EFCB34A7ECDC93F3D7E8516D44533DEAA2B3D8A2EAD108CCD321DB33E25C191C1116B7F46E0FCF69A6D5>
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http://purl.uniprot.org/SHA-384/5E6F275305B7EFCB34A7ECDC93F3D7E8516D44533DEAA2B3D8A2EAD108CCD321DB33E25C191C1116B7F46E0FCF69A6D5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5E6F275305B7EFCB34A7ECDC93F3D7E8516D44533DEAA2B3D8A2EAD108CCD321DB33E25C191C1116B7F46E0FCF69A6D5
http://www.w3.org/2000/01/rdf-schema#comment
"Large deletion of CYP21A2 gene could appear in 21-hydroxylase deficiency patients and the phenotype is similar to that of salt-wasting patients with heterozygous large deletion"
xsd:string
http://purl.uniprot.org/uniprot/#_020DA5E5802C134D22B3807C78EC177304ED7E20D26F58493053BDEE4BCD3A15D2F7375175B94246A70C53320437B54E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5E6F275305B7EFCB34A7ECDC93F3D7E8516D44533DEAA2B3D8A2EAD108CCD321DB33E25C191C1116B7F46E0FCF69A6D5
http://purl.uniprot.org/uniprot/P08686
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5E6F275305B7EFCB34A7ECDC93F3D7E8516D44533DEAA2B3D8A2EAD108CCD321DB33E25C191C1116B7F46E0FCF69A6D5
http://purl.uniprot.org/uniprot/#_P08686-mappedCitation-30917440
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5E6F275305B7EFCB34A7ECDC93F3D7E8516D44533DEAA2B3D8A2EAD108CCD321DB33E25C191C1116B7F46E0FCF69A6D5