@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE> .
@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:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_head {
  this: np:hasAssertion dgn-np:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_assertion;
    np:hasProvenance dgn-np:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_provenance;
    np:hasPublicationInfo dgn-np:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_assertion a np:Assertion .
  
  dgn-np:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_provenance a np:Provenance .
  
  dgn-np:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_assertion {
  miriam-gene:182 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNfd20b8752fbce81de28ad208b53832f1 sio:SIO_000628 miriam-gene:182, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_provenance {
  dgn-np:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_assertion dcterms:description
      "[To discover new candidate genes influencing glioma susceptibility, we conducted a principal component-adjusted genome-wide association study (GWAS) of 275,895 autosomal variants among 692 adult high-grade glioma cases (622 from the San Francisco Adult Glioma Study (AGS) and 70 from the Cancer Genome Atlas (TCGA)) and 3,992 controls (602 from AGS and 3,390 from Illumina iControlDB (iControls)).]. 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:19578366;
    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:NP692513.RAdB_VV191b1Ds3k07QnIFo9fVJvH6UQzAn0GSWxK3PZE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:00+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" .
}