Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_assertion> ?p ?o ?g. }
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- NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_assertion type Assertion NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_head.
- NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_assertion wasGeneratedBy ECO_0000203 NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_provenance.
- NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_assertion wasDerivedFrom befree-20140225 NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_provenance.
- NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_assertion SIO_000772 15689361 NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_provenance.
- NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_assertion evidence source_evidence_literature NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_provenance.
- NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_assertion description "[Of the cases where the CAPN3 gene was not affected, approximately 20% were diagnosed as LGMD2I muscular dystrophy, while facioscapulohumeral muscular dystrophy (FSHD) was uncommon in this sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676047.RAWqGUr9Q-Dko9mnAws3C1T735MLHG7xiG-RwJqArZOsw130_provenance.