@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec> .
@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:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_head {
  this: np:hasAssertion dgn-np:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_assertion;
    np:hasProvenance dgn-np:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_provenance;
    np:hasPublicationInfo dgn-np:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_assertion a np:Assertion .
  
  dgn-np:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_provenance a np:Provenance .
  
  dgn-np:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGN0005ab84b1a58d97f8673f8575c56f85 sio:SIO_000628 miriam-gene:4846, lld:C0027051;
    a sio:SIO_001121 .
}

dgn-np:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_provenance {
  dgn-np:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_assertion dcterms:description
      "[We screened 283 T2DM patients, inclusive of 160 with angiographically defined CAD, 73 with myocardial infarction (MI), 89 without MI and 121 T2DM individuals with no evidence of CAD for eNOS gene polymorphisms.]. 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:23182401;
    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:NP234191.RABNz8bFc4kRYQR-eKAmnjzK8LWkAx7Tw2mTlsgCM_8Ec130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:11+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" .
}