@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM> .
@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:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_head {
  this: np:hasAssertion dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_assertion ;
    np:hasProvenance dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_provenance ;
    np:hasPublicationInfo dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_assertion a np:Assertion .
  dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_provenance a np:Provenance .
  dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  lld:C0010068 a ncit:C7057 .
  dgn-gda:DGNe3a34098f1b9a9da1bbb41b664bb6942 sio:SIO_000628 miriam-gene:3949 , lld:C0010068 ;
    a sio:SIO_001121 .
}
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_provenance {
  dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_assertion dcterms:description "[The possible association of genetic markers at the apolipoprotein E (HhaI polymorphism), apolipoprotein B (XbaI, EcoRI and Ins/Del polymorphisms), and low-density lipoprotein receptor (LDLR) (AvaII, HincII and PvuII polymorphisms) with coronary artery disease (CAD) was evaluated in 50 Brazilian women with CAD diagnosed by angiography and in 100 healthy women (controls).]. 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:10958870 ;
    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:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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" .
}