Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.
- NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.
- NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_assertion evidence source_evidence_literature NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.
- NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_assertion SIO_000772 11810270 NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.
- NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_assertion wasDerivedFrom befree-2016 NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.
- NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_assertion wasGeneratedBy ECO_0000203 NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.
- befree-2016 importedOn "2016-02-19" NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.