@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk> .
@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:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_head {
  this: np:hasAssertion dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_assertion;
    np:hasProvenance dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_provenance;
    np:hasPublicationInfo dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_assertion a np:Assertion .
  
  dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_provenance a np:Provenance .
  
  dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0004943 a ncit:C7057 .
  
  dgn-gda:DGN8a03c6ffab8e1f885e2332a0ef9826e1 sio:SIO_000628 miriam-gene:4846, lld:C0004943;
    a sio:SIO_001121 .
}

dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_provenance {
  dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_assertion dcterms:description
      "[To assess potential associations between Korean Behçet's disease (BD) or other rheumatic diseases with vasculitis and two polymorphisms of the endothelial nitric oxide synthase (eNOS) gene, which include the Glu298Asp polymorphism in exon 7 and a variable number of tandem repeats (VNTR) polymorphism in intron 4.]. 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:14583572;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:08+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" .
}