Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_provenance.
- NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_assertion wasGeneratedBy ECO_0000203 NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_provenance.
- NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_assertion wasDerivedFrom befree-20140225 NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_provenance.
- NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_assertion SIO_000772 23942138 NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_provenance.
- NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_assertion evidence source_evidence_literature NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_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.
- befree-20140225 importedOn "2014-02-25" NP806548.RAwMzaa2NxlimjOT22bF6wUUU9F0CROzNmKvbiIBoWgWw130_provenance.