@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_head {
  this: np:hasAssertion dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_assertion;
    np:hasProvenance dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_provenance;
    np:hasPublicationInfo dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_assertion a np:Assertion .
  
  dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_provenance a np:Provenance .
  
  dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0007131 a ncit:C7057 .
  
  dgn-gda:DGN519e3436dd2f8eae72d6d02b56f68b88 sio:SIO_000628 miriam-gene:1312, lld:C0007131;
    a sio:SIO_001122 .
}

dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_provenance {
  dgn-np:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_assertion dcterms:description
      "[When we corrected for multiple testing using these statistical tools, three novel associations of NSCLC risk with SNPs in the CYP1B1 (Arg48Gly), COMT (Val158Met) and GSTT2 (Met139Ile) genes were found noteworthy.]. 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:18258609;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP654349.RArTqzLDF3lep9hpcoEAQU-yCdHyrJtUXTJXbZ7KBn2xs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:41+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}