Matches in Nanopublications for { ?s ?p "[Multiple logistic regression analysis showed the SLCO1B1 c.521T>C single-nucleotide polymorphism to be a significant risk factor (P = 0.009), with an odds ratio (OR) per variant allele of 2.06 (1.32-3.15) for all myopathy and 4.09 (2.06-8.16) for severe myopathy (CPK > 10× ULN, and/or rhabdomyolysis; n = 23).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP509881.RAu3y0k_XrAOO81-mZtca7vD8BYxRw7bUlI2HVwmbQdOQ130_assertion description "[Multiple logistic regression analysis showed the SLCO1B1 c.521T>C single-nucleotide polymorphism to be a significant risk factor (P = 0.009), with an odds ratio (OR) per variant allele of 2.06 (1.32-3.15) for all myopathy and 4.09 (2.06-8.16) for severe myopathy (CPK > 10× ULN, and/or rhabdomyolysis; n = 23).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509881.RAu3y0k_XrAOO81-mZtca7vD8BYxRw7bUlI2HVwmbQdOQ130_provenance.
- NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_assertion description "[Multiple logistic regression analysis showed the SLCO1B1 c.521T>C single-nucleotide polymorphism to be a significant risk factor (P = 0.009), with an odds ratio (OR) per variant allele of 2.06 (1.32-3.15) for all myopathy and 4.09 (2.06-8.16) for severe myopathy (CPK > 10× ULN, and/or rhabdomyolysis; n = 23).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_provenance.