@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8> .
@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:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_head {
  this: np:hasAssertion dgn-np:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_assertion ;
    np:hasProvenance dgn-np:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_provenance ;
    np:hasPublicationInfo dgn-np:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_assertion a np:Assertion .
  dgn-np:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_provenance a np:Provenance .
  dgn-np:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_assertion {
  miriam-gene:3667 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
  dgn-gda:DGN68a63dbad442920c7455cdfb7444677c sio:SIO_000628 miriam-gene:3667 , lld:C1956346 ;
    a sio:SIO_001122 .
}
dgn-np:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_provenance {
  dgn-np:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_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:NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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 ;
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    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}