Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.
- NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.
- NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_assertion evidence source_evidence_literature NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.
- NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_assertion SIO_000772 9217978 NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.
- NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_assertion wasDerivedFrom befree-20140225 NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.
- NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_assertion wasGeneratedBy ECO_0000203 NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP591810.RAcD0FApp0GDAVrdRq6egs_M3PwWoGiwbYdjykNHSraBM130_provenance.