@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_head {
  this: np:hasAssertion dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_assertion ;
    np:hasProvenance dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_provenance ;
    np:hasPublicationInfo dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_assertion a np:Assertion .
  dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_provenance a np:Provenance .
  dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  lld:C0027051 a ncit:C7057 .
  dgn-gda:DGNfc4684896afe750c8ff10a6daf73d26a sio:SIO_000628 miriam-gene:3075 , lld:C0027051 ;
    a sio:SIO_001122 .
}
dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_provenance {
  dgn-np:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_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-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP446337.RAws_8FbnElpF36oxzj_g6E3Ph9mJqIrw8sB_7A1lUTgI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:01+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}