Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance.
- NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_assertion wasGeneratedBy ECO_0000203 NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance.
- NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_assertion wasDerivedFrom befree-2016 NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance.
- NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_assertion SIO_000772 11485765 NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance.
- NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_assertion evidence source_evidence_literature NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance.
- NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_assertion description "[Peripherin/RDS gene mutation (Pro210Leu) and polymorphisms in Japanese patients with retinal dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325892.RA-kUh8gf7RrzUXfJxotj-fO-9EXcNfyXFXayMnFlDEcQ130_provenance.