Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.
- NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_assertion wasGeneratedBy ECO_0000203 NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.
- NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_assertion wasDerivedFrom befree-20150227 NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.
- NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_assertion SIO_000772 19339306 NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.
- NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_assertion evidence source_evidence_literature NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.
- NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.