@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_head {
  this: np:hasAssertion dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_assertion;
    np:hasProvenance dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_provenance;
    np:hasPublicationInfo dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_assertion a np:Assertion .
  
  dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_provenance a np:Provenance .
  
  dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_assertion {
  miriam-gene:255738 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN19c0fe6a3e4a50d5b880f9ad2b9c1706 sio:SIO_000628 miriam-gene:255738, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_provenance {
  dgn-np:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_assertion dcterms:description
      "[Our data support the concept that the rare allele of the R46L SNP at the PCSK9 locus significantly lowers LDL C, but does not greatly reduce CHD risk in an elderly population with a high prevalence of cardiovascular disease.]. 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:18262190;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP981791.RAzCIu4VPvJaLJCffj2oc4oSUPBFbKWj1QoBpC6pqCQKg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:40+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}