Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_assertion> ?p ?o ?g. }
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- NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_assertion type Assertion NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_head.
- NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_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." NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_provenance.
- NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_assertion evidence source_evidence_literature NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_provenance.
- NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_assertion SIO_000772 25186227 NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_provenance.
- NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_assertion wasDerivedFrom befree-2016 NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_provenance.
- NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_assertion wasGeneratedBy ECO_0000203 NP1216580.RAk_sCEskcVG7jyBt_Q__IJdXOs1VTKExpKN4wmf9hzK0130_provenance.