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DESCRIBE <http://purl.uniprot.org/SHA-384/D5E346918B8CF38FB7B67CA80B5F67C5B6F4A7A0A5C832B932BB93A2579FB28BD634FFB1D0DE27B2CB7050A4BBA5DFD6>
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http://purl.uniprot.org/SHA-384/D5E346918B8CF38FB7B67CA80B5F67C5B6F4A7A0A5C832B932BB93A2579FB28BD634FFB1D0DE27B2CB7050A4BBA5DFD6
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/D5E346918B8CF38FB7B67CA80B5F67C5B6F4A7A0A5C832B932BB93A2579FB28BD634FFB1D0DE27B2CB7050A4BBA5DFD6
http://www.w3.org/2000/01/rdf-schema#comment
"Mutations in MECP2 gene were found over 50% of patients with Rett syndrome in China."
xsd:string
http://purl.uniprot.org/uniprot/#_7E57E7E3581128A904717C1C4BF7C3D9A0CB1C78CB7001D8A41929762D1BD677C7639D2B078FCF7AB6E1548F23900879
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/D5E346918B8CF38FB7B67CA80B5F67C5B6F4A7A0A5C832B932BB93A2579FB28BD634FFB1D0DE27B2CB7050A4BBA5DFD6
http://purl.uniprot.org/uniprot/D3YJ43
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D5E346918B8CF38FB7B67CA80B5F67C5B6F4A7A0A5C832B932BB93A2579FB28BD634FFB1D0DE27B2CB7050A4BBA5DFD6
http://purl.uniprot.org/uniprot/#_D3YJ43-mappedCitation-12170461
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D5E346918B8CF38FB7B67CA80B5F67C5B6F4A7A0A5C832B932BB93A2579FB28BD634FFB1D0DE27B2CB7050A4BBA5DFD6