@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ> .
@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:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_head {
  this: np:hasAssertion dgn-np:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_assertion ;
    np:hasProvenance dgn-np:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_assertion a np:Assertion .
  dgn-np:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_provenance a np:Provenance .
  dgn-np:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_assertion {
  miriam-gene:1137 a ncit:C16612 .
  lld:C0085541 a ncit:C7057 .
  dgn-gda:DGNbdb9efd43c8add55b356738bc6d641b4 sio:SIO_000628 miriam-gene:1137 , lld:C0085541 ;
    a sio:SIO_001122 .
}
dgn-np:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_provenance {
  dgn-np:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_assertion dcterms:description "[Forty-six nocturnal frontal lobe epilepsy (NFLE) patients (in which the involvement of the CHRNA4 and CHRNB2 genes coding for neuronal nicotinic acetylcholine receptor (nAChRs) subunits associated to the disease were previously excluded) were analyzed for the presence of mutations in the CHRNA2 gene coding for the alpha2 subunit of the same receptor, which has been recently associated with the disease.]. 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:18226955 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP92657.RA_noLHudrx23V0N0IYcwTvUpwOINtyxx1Djo8WKU9FhQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:46+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" .
}