@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_head {
  this: np:hasAssertion dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_assertion ;
    np:hasProvenance dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_provenance ;
    np:hasPublicationInfo dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_assertion a np:Assertion .
  dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_provenance a np:Provenance .
  dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_assertion {
  miriam-gene:2741 a ncit:C16612 .
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dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_provenance {
  dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_assertion dcterms:description "[Understanding of the molecular basis of paroxysmal disorders affecting the central nervous system has been revolutionalized with the identification of mutations in genes for the neurotransmitter receptors, GLRA1 and CHRNA4, and a voltage-gated potassium channel, KCNA1, as causes of inherited neurological disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
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dgn-np:NP549237.RAzbknqtR7c7bwWsuudiclxnPlx2pjgsk_0vdZR8CDaFY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:31+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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}