Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance.
- NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_assertion description "[Hyperkalaemic periodic paralysis, paramyotonia congenita, and potassium-aggravated myotonia are three autosomal dominant skeletal muscle disorders linked to the SCN4A gene encoding the alpha-subunit of the human voltage-sensitive sodium channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance.
- NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_assertion evidence source_evidence_literature NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance.
- NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_assertion SIO_000772 10366610 NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance.
- NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_assertion wasDerivedFrom befree-2016 NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance.
- NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_assertion wasGeneratedBy ECO_0000203 NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance.
- befree-2016 importedOn "2016-02-19" NP254880.RAbr3H3edcdJ9dNfuep7Zm7YOeZ9ziJlHXV1B_3PyeSpg130_provenance.