Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_assertion> ?p ?o ?g. }
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- NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_assertion type Assertion NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_head.
- NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_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." NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_provenance.
- NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_assertion evidence source_evidence_literature NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_provenance.
- NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_assertion SIO_000772 22926674 NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_provenance.
- NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_assertion wasDerivedFrom befree-20150227 NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_provenance.
- NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_assertion wasGeneratedBy ECO_0000203 NP682846.RA4ckF5XxRqrlzQRxgYto6_ncjUoTBqZU8GaPHpzC9MRY130_provenance.