Matches in Nanopublications for { ?s ?p "[Because mutations in the COQ2 gene are associated with severe inherited myopathy, we hypothesized that common, mild genetic variation in COQ2 would be associated with inter-individual variation in statin intolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP887231.RARDJeBz8xhHwxk0rptkPlbSHTer28mofM-8_a_BE2Btg130_assertion description "[Because mutations in the COQ2 gene are associated with severe inherited myopathy, we hypothesized that common, mild genetic variation in COQ2 would be associated with inter-individual variation in statin intolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887231.RARDJeBz8xhHwxk0rptkPlbSHTer28mofM-8_a_BE2Btg130_provenance.
- NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_assertion description "[Because mutations in the COQ2 gene are associated with severe inherited myopathy, we hypothesized that common, mild genetic variation in COQ2 would be associated with inter-individual variation in statin intolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490131.RAO471ErEqChn7lQ4PWNQHVEEY6P6SK402sbxbXwBaHHU130_provenance.
- NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_assertion description "[Because mutations in the COQ2 gene are associated with severe inherited myopathy, we hypothesized that common, mild genetic variation in COQ2 would be associated with inter-individual variation in statin intolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600286.RA2biVtwf-Zwp2hU1flAF7BWqiVMHqMzV3cJFjDZHpTp4130_provenance.