Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.
- NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_assertion description "[Due to the unique role of 11-cis retinol dehydrogenase in the generation of visual pigments, it is a candidate gene for involvement in hereditary eye disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.
- NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_assertion evidence source_evidence_literature NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.
- NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_assertion SIO_000772 8884265 NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.
- NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_assertion wasDerivedFrom befree-2016 NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.
- NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_assertion wasGeneratedBy ECO_0000203 NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.