Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_assertion> ?p ?o ?g. }
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- NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_assertion type Assertion NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_head.
- NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_assertion description "[Although a clinical overlap between patients with dominant and recessive RYR1 mutations exists, in most cases with recessive mutations the pattern of muscle weakness is remarkably different from that observed in dominant CCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_provenance.
- NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_assertion evidence source_evidence_literature NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_provenance.
- NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_assertion SIO_000772 17483490 NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_provenance.
- NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_assertion wasDerivedFrom befree-20140225 NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_provenance.
- NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_assertion wasGeneratedBy ECO_0000203 NP616586.RAmZuwO30IAlW_4_rKprxPOn-y1ZSSwrzevPVt2haSjno130_provenance.