Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance.
- NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_assertion wasGeneratedBy ECO_0000203 NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance.
- NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_assertion wasDerivedFrom gad-20150221 NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance.
- NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_assertion SIO_000772 15051636 NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance.
- NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_assertion evidence source_evidence_literature NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance.
- NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_assertion description "[ LQTS-associated compound mutations cause a severe phenotype and are more common than expected. Individuals with compound mutations need to be identified, and their management should be tailored to their increased risk for arrhythmias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84578.RATq-9LSlHMMWc9XzeNrL42I_tJ7QnHUswb6aCqvpqzQY130_provenance.