@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4> .
@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:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_head {
  this: np:hasAssertion dgn-np:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_assertion;
    np:hasProvenance dgn-np:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_provenance;
    np:hasPublicationInfo dgn-np:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_assertion a np:Assertion .
  
  dgn-np:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_provenance a np:Provenance .
  
  dgn-np:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_assertion {
  miriam-gene:4899 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGN85285cd715ed74ac96cb089e5d3fb38c sio:SIO_000628 miriam-gene:4899, lld:C0038454;
    a sio:SIO_001121 .
}

dgn-np:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_provenance {
  dgn-np:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_assertion dcterms:description
      "[The Evaluation of Genomic Applications in Practice and Prevention Working Group (EWG) found insufficient evidence to recommend testing for the 9p21 genetic variant or 57 other variants in 28 genes (listed in ) to assess risk for cardiovascular disease (CVD) in the general population, specifically heart disease and stroke.]. 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:21042222;
    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:NP858299.RA6VEOL0WUM3sx1TE6wzT55TM-vt6CAGJL3f9lLeCHro4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:45+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" .
}