Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_assertion> ?p ?o ?g. }
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- NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_assertion type Assertion NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_head.
- NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_assertion description "[We conclude that allelic variants of MiRP1 contribute to a significant fraction of cases of drug-induced LQTS through multiple mechanisms and that common sequence variations that increase the risk of life-threatening drug reactions can be clinically silent before drug exposure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_provenance.
- NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_assertion evidence source_evidence_curated NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_provenance.
- NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_assertion SIO_000772 10984545 NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_provenance.
- NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_assertion wasDerivedFrom ctd_human-20130708 NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_provenance.
- NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_assertion wasGeneratedBy ECO_0000218 NP20762.RAv-IvXoO11hW0-3_LXFrCruVTRjv7RsW5mq29_Dzn_YU130_provenance.