Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_assertion> ?p ?o ?g. }
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- NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_assertion type Assertion NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_head.
- NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_provenance.
- NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_assertion evidence source_evidence_literature NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_provenance.
- NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_assertion SIO_000772 7650604 NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_provenance.
- NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_assertion wasDerivedFrom befree-20140225 NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_provenance.
- NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_assertion wasGeneratedBy ECO_0000203 NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_provenance.