Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance.
- NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_assertion description "[Our study confirms that the PROMM phenotype is associated with DM2-(CCTG)(n) expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance.
- NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_assertion evidence source_evidence_literature NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance.
- NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_assertion SIO_000772 15261229 NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance.
- NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_assertion wasDerivedFrom befree-20140225 NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance.
- NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_assertion wasGeneratedBy ECO_0000203 NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP891841.RAnZA6CJacv9LoaQXz7P8yGrchuPFRqzYBr4Ox1C0jRcc130_provenance.