Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance.
- NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_assertion description "[We evaluated patients with hereditary retinal diseases featuring subretinal spots (retinitis punctata albescens and fundus albipunctatus) and patients with typical dominant or recessive retinitis pigmentosa for mutations in RDH5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance.
- NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_assertion evidence source_evidence_literature NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance.
- NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_assertion SIO_000772 10369264 NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance.
- NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_assertion wasDerivedFrom befree-20150227 NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance.
- NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_assertion wasGeneratedBy ECO_0000203 NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP668483.RAGKCEdHZe36h0JOl3ctH3bYoTcyGGgYd44EzW0MgWvvg130_provenance.