@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_head {
  this: np:hasAssertion dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_assertion;
    np:hasProvenance dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_provenance;
    np:hasPublicationInfo dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_assertion a np:Assertion .
  
  dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_provenance a np:Provenance .
  
  dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_assertion {
  miriam-gene:4843 a ncit:C16612 .
  
  lld:C0018801 a ncit:C7057 .
  
  dgn-gda:DGNd10c25a1a196dae8b96bae0922ac7d11 sio:SIO_000628 miriam-gene:4843, lld:C0018801;
    a sio:SIO_001122 .
}

dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_provenance {
  dgn-np:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_assertion dcterms:description
      "[An association between polymorphism of iNOS gene (CCTTT)n, eNOS gene (Glu298Asp) with development of CHD and severity of CHF was shown. The polymorphism of eNOS gene (Glu298Asp) was associated with endothelial dysfunction.]. 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:20459417;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP175863.RAoTmz_xceRBKJPElW4iaLZVW_Ftri8zzNJB491m20048130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:07+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}