Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_assertion type Assertion NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_head.
- NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_assertion wasGeneratedBy ECO_0000203 NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_provenance.
- NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_assertion wasDerivedFrom befree-20140225 NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_provenance.
- NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_assertion SIO_000772 21545237 NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_provenance.
- NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_assertion evidence source_evidence_literature NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_provenance.
- NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_assertion description "[We report a novel G61R SOD1 mutation in a patient with a distinct phenotype including prominent lower motor neuron dysfunction, proximal weakness and atrophy with asymmetrical onset in the thigh and buttock and relentless clinical course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548856.RAgSGZmRGJtl_rCWw-Xn7xcZx7lcqaosJEyqeLM_7xK0g130_provenance.