Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance.
- NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_assertion description "[The numbers with 2, 1 and 0 APOL1 nephropathy risk variants, respectively, were 36, 17 and 20.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance.
- NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_assertion evidence source_evidence_literature NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance.
- NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_assertion SIO_000772 21931123 NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance.
- NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_assertion wasDerivedFrom befree-20140225 NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance.
- NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_assertion wasGeneratedBy ECO_0000203 NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP339750.RA9jK45nM9-mmo0BqIFHaBgWrDhqffm4S8VtWgfmX9BVI130_provenance.