Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance.
- NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_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." NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance.
- NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_assertion evidence source_evidence_literature NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance.
- NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_assertion SIO_000772 1639381 NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance.
- NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_assertion wasDerivedFrom befree-2016 NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance.
- NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_assertion wasGeneratedBy ECO_0000203 NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance.
- befree-2016 importedOn "2016-02-19" NP529528.RAJKEgl0doynkncsdR-xybj0zbQ5pCE_DMOSCxmR1G9Mw130_provenance.