Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance.
- NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance.
- NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_assertion evidence source_evidence_literature NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance.
- NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_assertion SIO_000772 18807109 NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance.
- NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_assertion wasDerivedFrom gad-20150221 NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance.
- NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_assertion wasGeneratedBy ECO_0000203 NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP130278.RAiqYfmX2A6clFj4C-hjfJHYrDrVuIBBOj11oiFBZIPjQ130_provenance.