Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_assertion> ?p ?o ?g. }
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- NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_assertion type Assertion NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_head.
- NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_assertion description "[Myotonic dystrophy (DM), the most common inherited muscle disorder, is caused by a CTG expansion in the 3-untranslated region of a protein kinase gene ( DMPK ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_provenance.
- NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_assertion evidence source_evidence_literature NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_provenance.
- NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_assertion SIO_000772 10332033 NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_provenance.
- NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_assertion wasDerivedFrom befree-2016 NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_provenance.
- NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_assertion wasGeneratedBy ECO_0000203 NP252929.RAnZfWPn2SJAni9UyZbp4iP6gx1cwCfmi3wTkrPLZxEik130_provenance.