Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion> ?p ?o ?g. }
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- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion type Assertion NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_head.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_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." NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion evidence source_evidence_literature NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion SIO_000772 7650604 NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion wasDerivedFrom befree-20140225 NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion wasGeneratedBy ECO_0000203 NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.