Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.
- NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_assertion description "[The present study is the first to report mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism whereby perturbations in GPD1-L precipitate a marked decrease in the peak sodium current and a potentially lethal BrS-like proarrhythmic substrate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.
- NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_assertion evidence source_evidence_literature NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.
- NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_assertion SIO_000772 17967976 NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.
- NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_assertion wasDerivedFrom befree-20150227 NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.
- NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_assertion wasGeneratedBy ECO_0000203 NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.
- befree-20150227 importedOn "2015-02-27" NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.