@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28> .
@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:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_head {
  this: np:hasAssertion dgn-np:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_assertion ;
    np:hasProvenance dgn-np:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_provenance ;
    np:hasPublicationInfo dgn-np:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_assertion a np:Assertion .
  dgn-np:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_provenance a np:Provenance .
  dgn-np:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_assertion {
  miriam-gene:3162 a ncit:C16612 .
  lld:C0027051 a ncit:C7057 .
  dgn-gda:DGN52f231e13955a14f3a87a63ae7cddebb sio:SIO_000628 miriam-gene:3162 , lld:C0027051 ;
    a sio:SIO_001121 .
}
dgn-np:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_provenance {
  dgn-np:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_assertion dcterms:description "[Cardiovascular risk profile and DNA samples for determination of the HO-1 genotype (carrier vs. noncarrier of a short (GT)n repeat allele) were obtained at baseline, and patients were followed for median 21 months for the occurrence of coronary events (myocardial infarction, percutaneous coronary interventions and coronary artery bypass graft), cerebrovascular events (stroke or carotid revascularization) and all-cause mortality.]. 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:16313248 ;
    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:NP228799.RAz99yesVV-em-WMELnNfMNOxv-IJM1OkttgxDHE6vX28130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:08+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" .
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}