@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw> .
@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:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_head {
   this: np:hasAssertion dgn-np:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_assertion ;
    np:hasProvenance dgn-np:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_provenance ;
    np:hasPublicationInfo dgn-np:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_assertion a np:Assertion .
  dgn-np:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_provenance a np:Provenance .
  dgn-np:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_assertion {
   miriam-gene:189 a ncit:C16612 .
  lld:C0010068 a ncit:C7057 .
  dgn-gda:DGNef65132f7557139c852a9bd82e9cb686 sio:SIO_000628 miriam-gene:189 , lld:C0010068 ;
    a sio:SIO_001121 .
}
dgn-np:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_provenance {
   dgn-np:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_assertion dcterms:description "[We correlated the published frequencies of susceptibility genotypes for the genes most often associated with CHD (ACE, AGT, APOE, F2, F5, MTHFR, PON1, and SERPINE1) with the incidence of the disease, controlling for the effects of smoking, systolic pressure, total cholesterol, and body-mass index.]. 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:17683517 ;
    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:NP772371.RALl9QD8DVFTTahSxa7lKkHw2j3qtVWTkR3A2ztWFoyKw130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:47+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> ;
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}