@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M> .
@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:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_head {
  this: np:hasAssertion dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_assertion ;
    np:hasProvenance dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_provenance ;
    np:hasPublicationInfo dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_assertion a np:Assertion .
  dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_provenance a np:Provenance .
  dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_assertion {
  miriam-gene:1139 a ncit:C16612 .
  lld:C0085541 a ncit:C7057 .
  dgn-gda:DGNdb2f6e368bacb9739fe47c22d3dd9245 sio:SIO_000628 miriam-gene:1139 , lld:C0085541 ;
    a sio:SIO_001121 .
}
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_provenance {
  dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_assertion dcterms:description "[It has been suggested that the homomer-forming α7 subunit (CHRNA7) of the neuronal nicotinic acetylcholine receptor (nAChR) is involved in the pathogenesis of common idiopathic generalized epilepsies (IGEs), whereas mutations of the gene coding for the α4 nAChR subunit (CHRNA4) are associated with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:23553139 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  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 ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:47+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}