Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP505402.RAt4MbLYOaSlIp9nl1W_za4PnDhT2n6TjXRm1CvQmKzB4130_provenance.