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- source_evidence_literature type ECO_0000212 NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_provenance.
- NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_assertion description "[This figure is comparable to the percentage of RP2 gene mutations that we have detected in our entire XLRP patient pool (10%-15%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_provenance.
- NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_assertion evidence source_evidence_literature NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_provenance.
- NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_assertion SIO_000772 10480356 NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_provenance.
- NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_assertion wasDerivedFrom befree-2016 NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_provenance.
- NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_assertion wasGeneratedBy ECO_0000203 NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_provenance.
- befree-2016 importedOn "2016-02-19" NP262512.RAUQztVgViguEkjQ3GpClkcum5jMZ8Ez9LEwptv087O4E130_provenance.