Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance.
- NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_assertion description "[Type I myotonic dystrophy (DM1) is caused by a triplet repeat expansion in the 3'-untranslated region (UTR) of the dystrophia myotonia protein kinase (DMPK) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance.
- NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_assertion evidence source_evidence_literature NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance.
- NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_assertion SIO_000772 18559347 NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance.
- NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_assertion wasDerivedFrom befree-20140225 NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance.
- NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_assertion wasGeneratedBy ECO_0000203 NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP923216.RAtrxTZULKKSwWYs7ITl4Jnw-NsUZ-lyPLbn5xtiQcApM130_provenance.