Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_assertion> ?p ?o ?g. }
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- NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_assertion type Assertion NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_head.
- NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_assertion description "[Myotonic dystrophy (DM) is caused by a defect in an unknown gene that maps to 19q13.3, flanked by the tightly linked markers ERCC1 on the proximal side and D19S51 on the distal side.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_provenance.
- NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_assertion evidence source_evidence_literature NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_provenance.
- NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_assertion SIO_000772 1639381 NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_provenance.
- NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_assertion wasDerivedFrom befree-20150227 NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_provenance.
- NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_assertion wasGeneratedBy ECO_0000203 NP381538.RABGJo99-mw_ws-J3z06o0aZcpM969fRNXRuMoGBDMva0130_provenance.