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DESCRIBE <http://purl.uniprot.org/SHA-384/CD05CA7BAC2E2A51346F1B46510582BCB4FA872BD565171E3B8D6952E47D1005CB887AD13E87FFCC9256BB6ADA804B49>
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http://purl.uniprot.org/SHA-384/CD05CA7BAC2E2A51346F1B46510582BCB4FA872BD565171E3B8D6952E47D1005CB887AD13E87FFCC9256BB6ADA804B49
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CD05CA7BAC2E2A51346F1B46510582BCB4FA872BD565171E3B8D6952E47D1005CB887AD13E87FFCC9256BB6ADA804B49
http://www.w3.org/2000/01/rdf-schema#comment
"Clinical Sequencing Solves a Diagnostic Dilemma by Identifying a Novel Pathogenic Variant in USB1 Gene Causing Poikiloderma with Neutropenia."
xsd:string
http://purl.uniprot.org/uniprot/#_5C9838784CDE5F807136B0ED56CF843F6496DD0C32F25C30759F60A5E8B560A366329A9724A6489B44110148D1BBE53D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CD05CA7BAC2E2A51346F1B46510582BCB4FA872BD565171E3B8D6952E47D1005CB887AD13E87FFCC9256BB6ADA804B49
http://purl.uniprot.org/uniprot/H3BNM8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CD05CA7BAC2E2A51346F1B46510582BCB4FA872BD565171E3B8D6952E47D1005CB887AD13E87FFCC9256BB6ADA804B49
http://purl.uniprot.org/uniprot/#_H3BNM8-mappedCitation-32936385
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CD05CA7BAC2E2A51346F1B46510582BCB4FA872BD565171E3B8D6952E47D1005CB887AD13E87FFCC9256BB6ADA804B49