Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_assertion> ?p ?o ?g. }
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- NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_provenance.
- NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_assertion evidence source_evidence_literature NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_provenance.
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- NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_assertion wasDerivedFrom befree-20140225 NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_provenance.
- NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_assertion wasGeneratedBy ECO_0000203 NP420166.RAgIgUpyxN22akBVXUO-xVDjJ2OVqsoFC-OmlD3zjh5J8130_provenance.