Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_assertion> ?p ?o ?g. }
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- NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_assertion type Assertion NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_head.
- NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_assertion description "[Disease worsened in patients with SCA1, SCA2, and SCA3 mutations (mean [SE] increase in CCFSw, +0.014 [0.005] to +0.025 [0.004] per year), improved in patients with SPG4 mutations (mean [SE] increase in CCFSw, -0.012 [0.003] per year; P = .02), and remained stable in patients with SCA6, SCA7, or other SCA mutations (mean [SE] increase in CCFSw, -0.015 [0.011] to +0.009 [0.013] per year) or hereditary spastic paraplegia with other SPG mutations (mean [SE] increase in CCFSw, -0.005 [0.005] per year).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_provenance.
- NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_assertion evidence source_evidence_literature NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_provenance.
- NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_assertion SIO_000772 22491195 NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_provenance.
- NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_assertion wasDerivedFrom befree-2016 NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_provenance.
- NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_assertion wasGeneratedBy ECO_0000203 NP973744.RAc9m08Vam8ebqxjY9ca64SP40GlvQPVt6cVJn_K4-EIA130_provenance.