Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.
- NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.
- NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_assertion evidence source_evidence_literature NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.
- NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_assertion SIO_000772 15596616 NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.
- NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_assertion wasDerivedFrom befree-2016 NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.
- NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_assertion wasGeneratedBy ECO_0000203 NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.
- befree-2016 importedOn "2016-02-19" NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_provenance.