@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI> .
@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:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_head {
  this: np:hasAssertion dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_assertion;
    np:hasProvenance dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_provenance;
    np:hasPublicationInfo dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_assertion a np:Assertion .
  
  dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_provenance a np:Provenance .
  
  dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN811acfd20914115c60937ddb40f82865 sio:SIO_000628 miriam-gene:2944, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_provenance {
  dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_assertion dcterms:description
      "[Recent studies suggest that the common variant in the GSTM1 and GSTT1 genes modifies the risk of coronary artery disease (CAD), however, it is unclear whether the risk of CAD modulated by variants in the GSTM1 and GSTT1 genes was associated with alterations of indices of oxidative stress and inflammation.]. 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:19823950;
    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:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+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" .
}