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- source_evidence_literature type ECO_0000212 NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.
- NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.
- NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_assertion evidence source_evidence_literature NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.
- NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_assertion SIO_000772 20346670 NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.
- NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_assertion wasDerivedFrom befree-2016 NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.
- NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_assertion wasGeneratedBy ECO_0000203 NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.
- befree-2016 importedOn "2016-02-19" NP802834.RAh2Nl_LGWyOUpEAalf_YYq9obhFIitYKcenTEeOYrkYE130_provenance.