Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_assertion> ?p ?o ?g. }
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- NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_assertion type Assertion NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_head.
- NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_assertion description "[Missense mutations in the AFG3L2 proteolytic domain account for ?1.5% of European autosomal dominant cerebellar ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_provenance.
- NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_assertion evidence source_evidence_literature NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_provenance.
- NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_assertion SIO_000772 20725928 NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_provenance.
- NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_assertion wasDerivedFrom befree-20150227 NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_provenance.
- NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_assertion wasGeneratedBy ECO_0000203 NP856458.RAgzu2UfIT1Wm9j9RVmyYpOVVgb7br-9oZRgwz56TPptQ130_provenance.