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- source_evidence_literature type ECO_0000212 NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_provenance.
- NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_assertion description "[The mutation causing myotonic dystrophy (DM) has recently been identified as an unstable CTG trinucleotide repeat located in the 3' untranslated region of a gene encoding for a protein with putative serine-threonine protein kinase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_provenance.
- NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_assertion evidence source_evidence_literature NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_provenance.
- NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_assertion SIO_000772 8499920 NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_provenance.
- NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_assertion wasDerivedFrom befree-2016 NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_provenance.
- NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_assertion wasGeneratedBy ECO_0000203 NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1343399.RAnHx3iujcN-EAmDVuO2sOvrCV82PCaPY-uoGlhFYWC7s130_provenance.