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- NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_assertion type Assertion NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_head.
- NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_assertion description "[These include lamin A/C in autosomal dominant Emery-Dreifuss muscular dystrophy, SMN in spinal muscular atrophy, SIX5 in myotonic dystrophy, calpain3 in type 2A limb-girdle muscular dystrophy, PABP2 in oculopharyngeal dystrophy, androgen receptor in spinal and bulbar muscular atrophy and the ataxins in hereditary ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_provenance.
- NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_assertion evidence source_evidence_literature NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_provenance.
- NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_assertion SIO_000772 10838245 NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_provenance.
- NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_assertion wasDerivedFrom befree-2016 NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_provenance.
- NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_assertion wasGeneratedBy ECO_0000203 NP285513.RAH5p9Yy6PAsBVsLp-EfOv-WkBew_fJzUyOPXCWWIjqdE130_provenance.