dgn-np:NP311785.RAAdUP4eKSChGTq9c3LxPvP1mo36tDHTzHcmwB6jYCbGg130_provenance {
  dgn-np:NP311785.RAAdUP4eKSChGTq9c3LxPvP1mo36tDHTzHcmwB6jYCbGg130_assertion dcterms:description "[Other important advances include recognition that genetic variants and mutations in the SLCO1B1, CYP and COQ2 genes may determine individual susceptibility to statin myopathy, and that statins may also initiate immune-mediated forms of necrotizing and inflammatory myopathy and unmask or aggravate various metabolic myopathies and other neuromuscular disorders.]. 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:20581681 ;
    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 .
}