Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_assertion> ?p ?o ?g. }
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- NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_assertion type Assertion NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_head.
- NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_assertion wasGeneratedBy ECO_0000203 NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_provenance.
- NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_assertion wasDerivedFrom befree-2016 NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_provenance.
- NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_assertion SIO_000772 12868501 NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_provenance.
- NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_assertion evidence source_evidence_literature NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_provenance.
- NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_assertion description "[We describe a patient with somatic mosaicism of a point mutation in the dystrophin gene causing benign muscular dystrophy with an unusual asymmetrical distribution of muscle weakness and contractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402282.RAmFyolr4xSDZpGpRE7hLHlYLVSCDIi7TTtcQERgkY2Yc130_provenance.