Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance.
- NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_assertion description "[Recent molecular studies of the original cases of normokalemic periodic paralysis (normoKPP) have raised suspicions that these families actually had hyperkalemic periodic paralysis (hyperKPP) due to mutations in the skeletal muscle sodium channel gene SCN4A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance.
- NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_assertion evidence source_evidence_literature NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance.
- NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_assertion SIO_000772 22926674 NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance.
- NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_assertion wasDerivedFrom befree-2016 NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance.
- NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_assertion wasGeneratedBy ECO_0000203 NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1008426.RA0NMG8erHkQJhxjpiD7TcGDnyeNGXol5Co_E6MIUeDDQ130_provenance.