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DESCRIBE <http://purl.uniprot.org/SHA-384/860732111F2E6A6990A5252CB60786CBCB0D88F58D974B61DD4735035F02771C4F34A97E0C10353B158F475F60945B99>
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http://purl.uniprot.org/SHA-384/860732111F2E6A6990A5252CB60786CBCB0D88F58D974B61DD4735035F02771C4F34A97E0C10353B158F475F60945B99
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/860732111F2E6A6990A5252CB60786CBCB0D88F58D974B61DD4735035F02771C4F34A97E0C10353B158F475F60945B99
http://www.w3.org/2000/01/rdf-schema#comment
"Missense mutations of the PRRT2 gene other than truncate and frameshift mutations were account for mild paroxysmal kinesigenic dyskinesia and/or infantile convulsions"
xsd:string
http://purl.uniprot.org/uniprot/#_68A44D5B2AD84321D38B3B25E09E98F2F308DBA496AA9097335E9D726182A3A46D1B78B4FAE07B4898C44B7A86E008E7
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/860732111F2E6A6990A5252CB60786CBCB0D88F58D974B61DD4735035F02771C4F34A97E0C10353B158F475F60945B99
http://purl.uniprot.org/uniprot/Q7Z6L0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/860732111F2E6A6990A5252CB60786CBCB0D88F58D974B61DD4735035F02771C4F34A97E0C10353B158F475F60945B99
http://purl.uniprot.org/uniprot/#_Q7Z6L0-mappedCitation-23063574
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/860732111F2E6A6990A5252CB60786CBCB0D88F58D974B61DD4735035F02771C4F34A97E0C10353B158F475F60945B99