@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4> .
@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:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_head {
  this: np:hasAssertion dgn-np:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_assertion;
    np:hasProvenance dgn-np:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_provenance;
    np:hasPublicationInfo dgn-np:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_assertion a np:Assertion .
  
  dgn-np:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_provenance a np:Provenance .
  
  dgn-np:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_assertion {
  miriam-gene:4843 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN397aad1ffe2d56b7c7ed37f1991b0b85 sio:SIO_000628 miriam-gene:4843, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_provenance {
  dgn-np:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_assertion dcterms:description
      "[Genetic variations in the NOS2 gene promoter and TLR4 coding sequence may lead to deleterious and protective effects, respectively, arising from altered function of the innate immune system in patients with T2DM.]. 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:19395279;
    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:NP53842.RAVSJNILd2b-L6fpLOUrfvPiKJFcbwdxTMCCysAswiIW4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}