Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_assertion> ?p ?o ?g. }
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- NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_assertion type Assertion NP472592.RA9fM9pgy7DvA3aBaHWmHa7xcUgcoWtZ9FYIYe7T7_bCg130_head.
- 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.