Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_assertion type Assertion NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_head.
- NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_assertion description "[PROMM (proximal myotonic myopathy) and DM2 (myotonic dystrophy Type 2) are autosomal dominant multisystem disorders that have both been linked to chromosome 3q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_provenance.
- NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_assertion evidence source_evidence_literature NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_provenance.
- NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_assertion SIO_000772 15261229 NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_provenance.
- NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_assertion wasDerivedFrom befree-20140225 NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_provenance.
- NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_assertion wasGeneratedBy ECO_0000203 NP927440.RAtx4LKg1KSHKnV9h1BwDdpR3YFCnBSZsBuKjEBFodAts130_provenance.