Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_assertion> ?p ?o ?g. }
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- NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_assertion type Assertion NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_head.
- NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_assertion wasGeneratedBy ECO_0000203 NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_provenance.
- NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_assertion wasDerivedFrom befree-2016 NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_provenance.
- NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_assertion SIO_000772 9354802 NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_provenance.
- NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_assertion evidence source_evidence_literature NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_provenance.
- NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_assertion description "[Because KVLQT1 mutations cause arrhythmia susceptibility in the long QT syndrome (LQT), we hypothesized that mutations in KCNE1 also cause this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1383190.RAx5APCii8SfpNL8oRme3AoVZFo1t-POdjutkD6tdfmS0130_provenance.