Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance.
- NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_assertion description "[Mutations in the human RDS gene are responsible for several forms of inherited blindness including autosomal-dominant retinitis pigmentosa and macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance.
- NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_assertion evidence source_evidence_literature NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance.
- NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_assertion SIO_000772 10704489 NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance.
- NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_assertion wasDerivedFrom befree-20140225 NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance.
- NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_assertion wasGeneratedBy ECO_0000203 NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP261436.RA8zvgNYMnkk5OHY3YAkn0zOYQ9lMhjzcjrY8NHVsN9iw130_provenance.