@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU> .
@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:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_head {
   this: np:hasAssertion dgn-np:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_assertion ;
    np:hasProvenance dgn-np:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_provenance ;
    np:hasPublicationInfo dgn-np:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_assertion a np:Assertion .
  dgn-np:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_provenance a np:Provenance .
  dgn-np:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_assertion {
   miriam-gene:2100 a ncit:C16612 .
  lld:C0027051 a ncit:C7057 .
  dgn-gda:DGN38a9a8ebf400659abace12647c6b9015 sio:SIO_000628 miriam-gene:2100 , lld:C0027051 ;
    a sio:SIO_001121 .
}
dgn-np:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_provenance {
   dgn-np:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_assertion dcterms:description "[Three polymorphisms of the ESR2 gene, and their associated haplotypes, were evaluated in 296 white women from the Women's Health Study and 566 white men from the Physicians' Health Study who developed CVD [myocardial infarction (MI) or ischemic stroke], each matched 1:1 to a member of the cohort study who remained free from CVD.]. 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:17702854 ;
    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:NP804536.RA4fkT1RjTQA1AETVxqgSbXHEnH_pBH04OSvQB276KmoU130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:13+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" .
}