Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_assertion> ?p ?o ?g. }
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- NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_assertion type Assertion NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_head.
- NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_assertion description "[These findings indicate that core myopathies are the most common form of congenital myopathies and that more than half can be attributed to RYR1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_provenance.
- NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_assertion evidence source_evidence_literature NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_provenance.
- NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_assertion SIO_000772 23394784 NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_provenance.
- NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_assertion wasDerivedFrom befree-20140225 NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_provenance.
- NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_assertion wasGeneratedBy ECO_0000203 NP498291.RAk9k5IN90-JYvmwsbYtTKwZw_w_8zRuVogngwl47OcGE130_provenance.