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DESCRIBE <http://purl.uniprot.org/SHA-384/D70BD9492EB1808EBDB47DB0DACCAFEC9BA608B525EA3135F0A826826D84286C22CE85427B8D79E19CFF898910C486D3>
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http://purl.uniprot.org/SHA-384/D70BD9492EB1808EBDB47DB0DACCAFEC9BA608B525EA3135F0A826826D84286C22CE85427B8D79E19CFF898910C486D3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/D70BD9492EB1808EBDB47DB0DACCAFEC9BA608B525EA3135F0A826826D84286C22CE85427B8D79E19CFF898910C486D3
http://www.w3.org/2000/01/rdf-schema#comment
"Different phenotypes of neurological diseases including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism caused by de novo ATP1A3 mutation in a family."
xsd:string
http://purl.uniprot.org/uniprot/#_CE561FA715E961E612938DF3B7DE2AFC86D11C5ED4360EFC3B127DA89DACF9778F34C6BFD97AAE51FE0BD0671CE7C01F
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/D70BD9492EB1808EBDB47DB0DACCAFEC9BA608B525EA3135F0A826826D84286C22CE85427B8D79E19CFF898910C486D3
http://purl.uniprot.org/uniprot/B3KNQ8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D70BD9492EB1808EBDB47DB0DACCAFEC9BA608B525EA3135F0A826826D84286C22CE85427B8D79E19CFF898910C486D3
http://purl.uniprot.org/uniprot/#_B3KNQ8-mappedCitation-34783933
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D70BD9492EB1808EBDB47DB0DACCAFEC9BA608B525EA3135F0A826826D84286C22CE85427B8D79E19CFF898910C486D3