@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU> .
@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:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_head {
  this: np:hasAssertion dgn-np:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_assertion;
    np:hasProvenance dgn-np:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_provenance;
    np:hasPublicationInfo dgn-np:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_assertion a np:Assertion .
  
  dgn-np:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_provenance a np:Provenance .
  
  dgn-np:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_assertion {
  miriam-gene:182 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGN17069ad33c009202b7f26f26da5c8223 sio:SIO_000628 miriam-gene:182, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_provenance {
  dgn-np:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_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:NP906381.RAGsDCPuWsIDluPC5iwLjHY1OTFnyKUR6R4bk853stVPU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:16+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" .
}