Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance.
- NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_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." NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance.
- NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_assertion evidence source_evidence_literature NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance.
- NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_assertion SIO_000772 7152518 NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance.
- NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_assertion wasDerivedFrom befree-20140225 NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance.
- NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_assertion wasGeneratedBy ECO_0000203 NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance.