@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU> .
@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 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:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_head {
  this: np:hasAssertion dgn-np:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_assertion;
    np:hasProvenance dgn-np:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_provenance;
    np:hasPublicationInfo dgn-np:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_assertion a np:Assertion .
  
  dgn-np:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_provenance a np:Provenance .
  
  dgn-np:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_assertion {
  miriam-gene:7099 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNfd13990445ba6e5008825005f3c47e83 sio:SIO_000628 miriam-gene:7099, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_provenance {
  dgn-np:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_assertion dct: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:NP80683.RA5ZLzvx6uVPi13vPxdVHsa_7Xn2MPcA6Hn2cFYxDlqiU130_publicationInfo {
  this: dct:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}