@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM> .
@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:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_head {
  this: np:hasAssertion dgn-np:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_assertion ;
    np:hasProvenance dgn-np:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_provenance ;
    np:hasPublicationInfo dgn-np:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_assertion a np:Assertion .
  dgn-np:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_provenance a np:Provenance .
  dgn-np:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  lld:C0042373 a ncit:C7057 .
  dgn-gda:DGNdc6739829cf3c683fe4b966f4efb1710 sio:SIO_000628 miriam-gene:3075 , lld:C0042373 ;
    a sio:SIO_001121 .
}
dgn-np:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_provenance {
  dgn-np:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_assertion dcterms:description "[We, therefore, evaluated the CFH genetic variant Y402H amongst 685 Caucasian individuals who subsequently developed arterial or venous thrombotic event (incident myocardial infarction (MI), ischaemic stroke, or venous thromboembolism) and amongst 685 age- and smoking-matched Caucasian individuals who remained free of reported vascular disease during follow-up (controls) within the Physicians' Health Study cohort.]. 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:16229850 ;
    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:NP244599.RAD7LGQlRrZh2gr-2GYEjoeOK9brfo1kx58eB6FG9YlKM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:17+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> ;
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}