@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U> .
@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:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_head {
  this: np:hasAssertion dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_assertion;
    np:hasProvenance dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_provenance;
    np:hasPublicationInfo dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_assertion a np:Assertion .
  
  dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_provenance a np:Provenance .
  
  dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_assertion {
  miriam-gene:6387 a ncit:C16612 .
  
  lld:C0004153 a ncit:C7057 .
  
  dgn-gda:DGNc3d3b1bea059fdf55da7fdfbad849686 sio:SIO_000628 miriam-gene:6387, lld:C0004153;
    a sio:SIO_001121 .
}

dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_provenance {
  dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_assertion dcterms:description
      "[However, no significant differences in genotypic and allelic frequencies between RA patients with and without CV events were observed, as was also the case when values of surrogate markers of atherosclerosis were assessed according to CXCL12 rs501120 genotype frequencies.]. 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:22386691;
    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:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:35+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" .
}