Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance.
- NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_assertion description "[Myotonic dystrophy type 1 (DM1) is a debilitating multisystemic disorder caused by a CTG repeat expansion in the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance.
- NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_assertion evidence source_evidence_literature NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance.
- NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_assertion SIO_000772 15972723 NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance.
- NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_assertion wasDerivedFrom befree-2016 NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance.
- NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_assertion wasGeneratedBy ECO_0000203 NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance.
- befree-2016 importedOn "2016-02-19" NP500598.RAg0rYgze0XbF-LnDp21rxHsl6KBsMnFke_4uL7Y1AZoM130_provenance.