Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.
- NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_assertion description "[Multiple families, predominantly of German descent and with clinically variable presentation that included proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed linkage to the 3q21 region and were recently shown to segregate a (CCTG)(n) expansion mutation in intron 1 of ZNF9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.
- NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_assertion evidence source_evidence_literature NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.
- NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_assertion SIO_000772 12970845 NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.
- NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_assertion wasDerivedFrom befree-20140225 NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.
- NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_assertion wasGeneratedBy ECO_0000203 NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722716.RA5_gOy9OB0MbccKZUaJz7dIJYBka4YVnxt4_uVOC1WBk130_provenance.