Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1124660.RAn5ttUdLUQhShVbsPO9bqCRujBMyOL5pFzeOtm05qlEM#assertion> ?p ?o ?g. }
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- assertion description "[Myotonic dystrophy type 2 (DM2) is an autosomal dominant inherited disorder with (CCTG)n repeat expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 25186227 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.