@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc> .
@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:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_head {
  this: np:hasAssertion dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_assertion;
    np:hasProvenance dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_provenance;
    np:hasPublicationInfo dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_assertion a np:Assertion .
  
  dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_provenance a np:Provenance .
  
  dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_assertion {
  miriam-gene:7099 a ncit:C16612 .
  
  lld:C0948480 a ncit:C7057 .
  
  dgn-gda:DGN3af8cb589c793c136811a9334f95337a sio:SIO_000628 miriam-gene:7099, lld:C0948480;
    a sio:SIO_001122 .
}

dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_provenance {
  dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_assertion dcterms:description
      "[Although inflammation has been implicated in the pathophysiology of restenosis, the 896A/G and 1196C/T polymorphisms or haplotypes based on these polymorphisms at the TLR4 locus are not associated with an increased risk of target vessel revascularization or angiographic restenosis after PCI. These polymorphisms are not useful for pre-PCI identification of patients at risk for restenosis.]. 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:20671584;
    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:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:45+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" .
}