@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M> .
@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:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_head {
  this: np:hasAssertion dgn-np:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_assertion ;
    np:hasProvenance dgn-np:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_provenance ;
    np:hasPublicationInfo dgn-np:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_assertion a np:Assertion .
  dgn-np:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_provenance a np:Provenance .
  dgn-np:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  lld:C0040038 a ncit:C7057 .
  dgn-gda:DGN15ebe66fdd7a9186b1632a60f4e4f5e0 sio:SIO_000628 miriam-gene:3075 , lld:C0040038 ;
    a sio:SIO_001122 .
}
dgn-np:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_provenance {
  dgn-np:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_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:NP446387.RAyjnleyne1mEuZcZxCgHSUlsVFUUk2gZEo8h4mnKkp6M130_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" .
}