@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg> .
@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:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_head {
  this: np:hasAssertion dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_assertion ;
    np:hasProvenance dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_provenance ;
    np:hasPublicationInfo dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_assertion a np:Assertion .
  dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_provenance a np:Provenance .
  dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
  dgn-gda:DGN69a8aef5fd131ea28bf5e0f9471ba2d1 sio:SIO_000628 miriam-gene:3949 , lld:C1956346 ;
    a sio:SIO_001122 .
}
dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_provenance {
  dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_assertion dcterms:description "[A genetic risk score based on nine genetic variants independently associated with CAD irrespective of other cardiovascular risk factors was associated with the presence of the disease. Cohort studies are needed to determine whether this genetic risk score can improve the predictive capacity or the risk classification of classical risk functions.]. 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:20738937 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}