Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_assertion> ?p ?o ?g. }
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- NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_assertion type Assertion NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_head.
- NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_assertion description "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance.
- NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_assertion evidence source_evidence_literature NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance.
- NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_assertion SIO_000772 17467628 NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance.
- NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_assertion wasDerivedFrom befree-20140225 NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance.
- NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_assertion wasGeneratedBy ECO_0000203 NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance.