Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance.
- NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_assertion description "[The mutations in PRPH2 account for 10.3% of adRP in the French population, which is higher than previously reported (0%-8%) This makes PRPH2 the second most frequent adRP gene after RHO in our series.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance.
- NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_assertion evidence source_evidence_literature NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance.
- NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_assertion SIO_000772 25447119 NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance.
- NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_assertion wasDerivedFrom befree-2016 NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance.
- NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_assertion wasGeneratedBy ECO_0000203 NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1242163.RAZqUJ0Hfp8V5Sc9Ni9xw4BjWwsB9XRsNvdmtfmIvnGt8130_provenance.