Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance.
- NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_assertion description "[It has recently been shown that mutations in RDH12, encoding a retinol dehydrogenase, result in severe and early-onset autosomal recessive retinal dystrophy (arRD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance.
- NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_assertion evidence source_evidence_literature NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance.
- NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_assertion SIO_000772 16269441 NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance.
- NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_assertion wasDerivedFrom befree-20140225 NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance.
- NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_assertion wasGeneratedBy ECO_0000203 NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP624753.RAQtWeM6tVNu9ZqigDe8CaLHNP1lzQOSWI7a_nTfs3iKg130_provenance.