Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_assertion> ?p ?o ?g. }
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- NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_assertion type Assertion NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_head.
- NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_assertion description "[Progression was faster in patients with SCA2 mutations and normal alleles with 22 or fewer repeats (P = .02) and in patients with SCA3 mutations with parkinsonism and/or dystonia at baseline (P = .003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_provenance.
- NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_assertion evidence source_evidence_literature NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_provenance.
- NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_assertion SIO_000772 22491195 NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_provenance.
- NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_assertion wasDerivedFrom befree-20150227 NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_provenance.
- NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_assertion wasGeneratedBy ECO_0000203 NP541687.RAYP-wYjQGwH7T0MKCE4RyUCsMWlUJmCILtZTtE1HYIQ0130_provenance.