Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_assertion> ?p ?o ?g. }
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- NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_assertion type Assertion NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_head.
- NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_assertion description "[Dysregulation of calcium signals because of defects of the skeletal muscle sarcoplasmic reticulum calcium release channel (ryanodine receptor; RyR1) is causative of several congenital muscle disorders including malignant hyperthermia (MH; MIM #145600), central core disease (CCD; MIM #11700), specific forms of multi-minicore disease (MmD; MIM # 255320) and centronuclear myopathy (CNM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_provenance.
- NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_assertion evidence source_evidence_literature NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_provenance.
- NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_assertion SIO_000772 18313359 NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_provenance.
- NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_assertion wasDerivedFrom befree-20140225 NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_provenance.
- NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_assertion wasGeneratedBy ECO_0000203 NP865065.RAjn_lsiLwmGpbiVCp08Can1Qs7fe7h7gsyd6SIq7jWNY130_provenance.