@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8> .
@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:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_head {
  this: np:hasAssertion dgn-np:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_assertion;
    np:hasProvenance dgn-np:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance;
    np:hasPublicationInfo dgn-np:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_assertion a np:Assertion .
  
  dgn-np:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance a np:Provenance .
  
  dgn-np:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_assertion {
  miriam-gene:2703 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGNf0874680c0b933e6aae5761419533c3e sio:SIO_000628 miriam-gene:2703, lld:C1956346;
    a sio:SIO_001121 .
}

dgn-np:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_provenance {
  dgn-np:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_assertion dcterms:description
      "[We tested the impact of genetic risk score (GRS(24SNP/CAD)) calculated as a weighted (by allelic odds ratios for CAD) sum of CAD risk alleles from the studied 24 variants on CIMT, CAE, the incidence of carotid atherosclerosis and the progression of CIMT and CAE during a 6-year follow-up.]. 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:22295058;
    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:NP615122.RAJS9s2RIagGz-llZkcH1pOMb1ES0jHE5K1EaPB_0MP-8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:12+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" .
}