Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance.
- NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_assertion description "[These results do not define a clear cataract-SORD deficiency etiopathogenic relationship, nevertheless, they strongly suggest activity polymorphism in human red cell SORD, which would be highly relevant not only to the study of cataracts but of other major complications in diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance.
- NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_assertion evidence source_evidence_literature NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance.
- NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_assertion SIO_000772 7152518 NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance.
- NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_assertion wasDerivedFrom befree-20140225 NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance.
- NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_assertion wasGeneratedBy ECO_0000203 NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance.