@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA> .
@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:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_head {
  this: np:hasAssertion dgn-np:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_assertion;
    np:hasProvenance dgn-np:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_provenance;
    np:hasPublicationInfo dgn-np:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_assertion a np:Assertion .
  
  dgn-np:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_provenance a np:Provenance .
  
  dgn-np:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN82e2467929c27793d2154a3f9b3057f7 sio:SIO_000628 miriam-gene:4846, lld:C0024141;
    a sio:SIO_001122 .
}

dgn-np:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_provenance {
  dgn-np:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_assertion dcterms:description
      "[The purpose of this study was to analyse the effect of the T-786C polymorphism and intron 4 27 bp variable number tandem repeat(VNTR) eNOS markers for their potential association with Systemic Lupus Erythematosus(SLE), Hashimotos thyroiditis(HT) and Rheumatoid arthritis(RA) as well as to explore their effect on eNOS mRNA expression and nitrate production(NOx).]. 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:23481632;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1059664.RApmAbjieqaNpGCnzDn6dB5Q0KeGiC4E1MhqLKSGqQDjA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:46+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" .
}