Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance.
- NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_assertion description "[Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance.
- NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_assertion evidence source_evidence_literature NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance.
- NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_assertion SIO_000772 19818506 NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance.
- NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_assertion wasDerivedFrom befree-2016 NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance.
- NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_assertion wasGeneratedBy ECO_0000203 NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance.
- befree-2016 importedOn "2016-02-19" NP768617.RAjgorwT0QKU6kQdth4OeBuKAazbauQFLroSm5N08OjCU130_provenance.