SPARQL
Downloads
Documentation/Help
Skip Header
Results
Your Query
Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/AFA7546A5293A8EDE5B8582C6C4CD83B1254B1E6CCB5C6A2098ABC0E4A30CE8049B34D5719BCB3639CFAC0DA2A837FF9>
Submit Query
Cancel
RDF/XML
NTriples
Turtle
Show query
Share
Subject
Predicate
Object
http://purl.uniprot.org/SHA-384/AFA7546A5293A8EDE5B8582C6C4CD83B1254B1E6CCB5C6A2098ABC0E4A30CE8049B34D5719BCB3639CFAC0DA2A837FF9
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/AFA7546A5293A8EDE5B8582C6C4CD83B1254B1E6CCB5C6A2098ABC0E4A30CE8049B34D5719BCB3639CFAC0DA2A837FF9
http://www.w3.org/2000/01/rdf-schema#comment
"We conclude that exon-disrupting deletions of NRXN1 represent a genetic risk factor in the genetically complex predisposition of common idiopathic generalized epilepsies"
xsd:string
http://purl.uniprot.org/uniprot/#_EB5B61ACB95487AF7DBBDC93DD98BE8D120C005DF77D9A060E2BB64E2B073CEDD539AF1E8B09DE25B6F5C52439BA25B6
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/AFA7546A5293A8EDE5B8582C6C4CD83B1254B1E6CCB5C6A2098ABC0E4A30CE8049B34D5719BCB3639CFAC0DA2A837FF9
http://purl.uniprot.org/uniprot/H7BYC7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AFA7546A5293A8EDE5B8582C6C4CD83B1254B1E6CCB5C6A2098ABC0E4A30CE8049B34D5719BCB3639CFAC0DA2A837FF9
http://purl.uniprot.org/uniprot/#_H7BYC7-mappedCitation-23294455
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/AFA7546A5293A8EDE5B8582C6C4CD83B1254B1E6CCB5C6A2098ABC0E4A30CE8049B34D5719BCB3639CFAC0DA2A837FF9