http://rdf.disgenet.org/resource/nanopub/NP821803.RAchHQve7OxIDrArR4YaYy4xVLpJAV15xMCgjQxADpO0k
type: Nanopublication
created: 2016-05-13T12:47:57+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetv3.0rdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v4.0.0.0

http://rdf.disgenet.org/resource/nanopub/NP821803.RAchHQve7OxIDrArR4YaYy4xVLpJAV15xMCgjQxADpO0k130_assertion
type: Assertion
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.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20581681
was generated by: ECO_0000203

befree-2016
imported on: 2016-02-19

DisGeNET evidence - LITERATURE
type: ECO_0000212
comment: Gene-disease associations inferred from text-mining the literature.

disgenetv3.0rdf
version: v4.0.0