Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance.
- NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_assertion description "[One patient had compound heterozygous mutations in RDH5 and suffered from FAP with mild maculopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance.
- NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_assertion evidence source_evidence_literature NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance.
- NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_assertion SIO_000772 22559933 NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance.
- NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_assertion wasDerivedFrom befree-20140225 NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance.
- NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_assertion wasGeneratedBy ECO_0000203 NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP673278.RAcyDhSDKW6IYcurxJmMWg8h8L8iFPE1RXB3Ea01nJ3Bo130_provenance.