@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow> .
@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:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_head {
  this: np:hasAssertion dgn-np:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_assertion ;
    np:hasProvenance dgn-np:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_provenance ;
    np:hasPublicationInfo dgn-np:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_assertion a np:Assertion .
  dgn-np:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_provenance a np:Provenance .
  dgn-np:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_assertion {
  miriam-gene:1135 a ncit:C16612 .
  lld:C0085541 a ncit:C7057 .
  dgn-gda:DGN69c361d1b499ae0162a61955155895db sio:SIO_000628 miriam-gene:1135 , lld:C0085541 ;
    a sio:SIO_001121 .
}
dgn-np:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_provenance {
  dgn-np:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_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: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:NP514850.RAcruQHDmrrAsk5MbMHkuowlFf5dctsvMIttG7kYx__ow130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:07+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" .
}