Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance.
- NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_assertion description "[It has recently been shown that mutations in RDH12, encoding a retinol dehydrogenase, result in severe and early-onset autosomal recessive retinal dystrophy (arRD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance.
- NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_assertion evidence source_evidence_literature NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance.
- NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_assertion SIO_000772 16269441 NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance.
- NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_assertion wasDerivedFrom befree-20140225 NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance.
- NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_assertion wasGeneratedBy ECO_0000203 NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP227474.RAqQkwyv0x1n82XvhqoK_X578xER6mi0h8pOWv48QZ9gY130_provenance.