Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_assertion> ?p ?o ?g. }
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- NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_assertion type Assertion NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_head.
- NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_assertion description "[Over the past 2 decades, a number of inherited cardiac arrhythmias, including congenital long QT syndrome (LQTS) and Brugada syndrome (BrS), have been shown to have a link to mutations in genes encoding for ion channels or other membrane components.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_provenance.
- NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_assertion evidence source_evidence_literature NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_provenance.
- NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_assertion SIO_000772 24200848 NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_provenance.
- NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_assertion wasDerivedFrom befree-2016 NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_provenance.
- NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_assertion wasGeneratedBy ECO_0000203 NP1125753.RA9HnCg0nUWCNHu66jHffUZM7yUVISNOmXN4B-tXk_X14130_provenance.