Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_assertion> ?p ?o ?g. }
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- NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_assertion type Assertion NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_head.
- NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_assertion wasGeneratedBy ECO_0000203 NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_provenance.
- NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_assertion wasDerivedFrom befree-2016 NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_provenance.
- NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_assertion SIO_000772 12621127 NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_provenance.
- NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_assertion evidence source_evidence_literature NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_provenance.
- NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_assertion description "[Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386007.RAYsdaYcT8MSh2DVGMhas82bvqyWx9CQ2JtkAWKGcYTz0130_provenance.