Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_assertion> ?p ?o ?g. }
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- NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_assertion type Assertion NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_head.
- NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_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." NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_provenance.
- NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_assertion evidence source_evidence_literature NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_provenance.
- NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_assertion SIO_000772 10366610 NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_provenance.
- NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_assertion wasDerivedFrom befree-20140225 NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_provenance.
- NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_assertion wasGeneratedBy ECO_0000203 NP550223.RAQGWZl6P35ySOG-8EovRHN58FlJZkJiTad9TzXwRK3wg130_provenance.