@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4> .
@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:NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4130_head {
  this: np:hasAssertion dgn-np:NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4130_assertion;
    np:hasProvenance dgn-np:NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4130_provenance;
    np:hasPublicationInfo dgn-np:NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4130_publicationInfo a
      np:PublicationInfo .
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dgn-np:NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0242339 a ncit:C7057 .
  
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dgn-np:NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4130_provenance {
  dgn-np:NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4130_assertion dcterms:description
      "[We found several synergistic effects between the studied polymorphisms and classical risk factors such as hypertension, obesity, diabetes and dyslipidaemia: the presence of the DD genotype of ACE I/D (and also ACE11860 GG) increases the odds of developing CAD when associated to each one of these classical risk factors, particularly when considering the male and early onset CAD subgroup analysis; AGT235 TT also increases the CAD risk in the presence of hypertension and dyslipidaemia, and AT1R1166 interacts positively with hypertension, smoking and obesity.]. 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:18637188;
    prov:wasDerivedFrom dgn-void:befree-20140225;
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  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:NP405853.RAWuiQHXO1Hi9gwyfSx4VjFRM4T0mwrdDrKCDCAZUsQV4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:01+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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    prv:usedData dgn-void:disgenetrdf;
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