Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_assertion> ?p ?o ?g. }
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- NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_assertion type Assertion NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_head.
- NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_assertion description "[More than 200 variants in RyR1 have been identified in DNA from patients with malignant hyperthermia (MH) and congenital myopathies; only 30 have been sufficiently studied so as to be identified as MH-causative mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_provenance.
- NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_assertion evidence source_evidence_literature NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_provenance.
- NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_assertion SIO_000772 21926372 NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_provenance.
- NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_assertion wasDerivedFrom befree-2016 NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_provenance.
- NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_assertion wasGeneratedBy ECO_0000203 NP924490.RA0S6qvlnLe4TtUABWoiPJpU05Q-ZqwZRbbyaoMrj_VGk130_provenance.