@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI> .
@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:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_head {
  this: np:hasAssertion dgn-np:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_assertion;
    np:hasProvenance dgn-np:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_provenance;
    np:hasPublicationInfo dgn-np:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_assertion a np:Assertion .
  
  dgn-np:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_provenance a np:Provenance .
  
  dgn-np:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_assertion {
  miriam-gene:7099 a ncit:C16612 .
  
  lld:C0004153 a ncit:C7057 .
  
  dgn-gda:DGNfe731daf23305cef8fc4c8948f346132 sio:SIO_000628 miriam-gene:7099, lld:C0004153;
    a sio:SIO_001122 .
}

dgn-np:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_provenance {
  dgn-np:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_assertion dcterms:description
      "[Because atherosclerosis is an inflammatory process apparently modulated by chronic infections, we studied the effect of single nucleotide polymorphisms (SNPs) in TLR4 and CD14 on the extent of clinically relevant atherosclerosis in patients with peripheral arterial disease (PAD).]. 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:16890863;
    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:NP50425.RA9TgZrVES_nYdslkS862ebYPhu7zpsRfW-a6t0SjD2RI130_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" .
}