@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc> .
@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:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_head {
  this: np:hasAssertion dgn-np:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_assertion;
    np:hasProvenance dgn-np:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_provenance;
    np:hasPublicationInfo dgn-np:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_assertion a np:Assertion .
  
  dgn-np:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_provenance a np:Provenance .
  
  dgn-np:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_assertion {
  miriam-gene:23771 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGN9e1ef9e2a10c7f13c4b6711991a3eb4a sio:SIO_000628 miriam-gene:23771, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_provenance {
  dgn-np:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_assertion dcterms:description
      "[Because ACE insertion/deletion (I/D) polymorphism has been shown to be associated with diabetes, hypertension, coronary artery diseases, and diabetic nephropathy, and because plasma ACE concentration has been found to be associated with plasma triglyceride and total cholesterol levels in patients with type 2 diabetes, the goal of this study was to investigate whether ACE gene I/D polymorphism is associated with metabolic syndrome in Chinese subjects with type 2 diabetes.]. 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:12032106;
    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:NP471900.RAV72wxAytenF9Fl6s79bFLcL-44SvIJ4K6GrgN4nc3Mc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:43+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" .
}