@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ> .
@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#> .
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  this: np:hasAssertion dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_assertion ;
    np:hasProvenance dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_assertion a np:Assertion .
  dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_provenance a np:Provenance .
  dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_assertion {
  miriam-gene:1137 a ncit:C16612 .
  lld:C0270853 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_provenance {
  dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_assertion dcterms:description "[In the present study, we examined the possible role of CHRNA4 in common subtypes of idiopathic generalized epilepsy (IGE), comprising childhood and juvenile absence epilepsy and juvenile myoclonic epilepsy (JME), by systematically screening the coding region of the gene for sequence variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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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 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:54+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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