Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance.
- NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_assertion wasGeneratedBy ECO_0000203 NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance.
- NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_assertion wasDerivedFrom befree-20150227 NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance.
- NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_assertion SIO_000772 11448300 NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance.
- NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_assertion evidence source_evidence_literature NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance.
- NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_assertion description "[Machado-Joseph disease-SCA3 was the most common type of autosomal dominant SCA in the Taiwanese cohort, accounting for 35 cases (47.3%), followed by SCA6 (8 [10.8%]), SCA2 (8 [10.8%]), SCA1 (4 [5.4%]), SCA7 (2 [2.7%]), dentatorubropallidoluysian atrophy (1 [1.4%]), and SCA8 (0%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681938.RAE56QI9gpcIeH3_k38EMX74gy5TuQIsyFIT_Cw66jBgk130_provenance.