@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo> .
@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:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_head {
  this: np:hasAssertion dgn-np:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_assertion;
    np:hasProvenance dgn-np:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_provenance;
    np:hasPublicationInfo dgn-np:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_assertion a np:Assertion .
  
  dgn-np:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_provenance a np:Provenance .
  
  dgn-np:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_assertion {
  miriam-gene:5243 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN1ca1e25f3c181e691a00fc58f82dafb1 sio:SIO_000628 miriam-gene:5243, lld:C0014544;
    a sio:SIO_001122 .
}

dgn-np:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_provenance {
  dgn-np:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_assertion dcterms:description
      "[We performed a meta-analysis to evaluate the association between ABCB1 C3435T polymorphisms and the prevalence of epilepsy, including all relevant human studies (until June 2009), in which patients with or without epilepsy had undergone genotyping for the ABCB1 gene.]. 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:20491876;
    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:NP49820.RAvWhPepM43es-VQKzR9FwmriSglyUxRcpHyrguGk-UNo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}