Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance.
- NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_assertion description "[Heterozygous mutations in BEST1 have previously been found to cause the two dominantly inherited disorders, Best macular dystrophy and autosomal-dominant vitreoretinochoroidopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance.
- NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_assertion evidence source_evidence_literature NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance.
- NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_assertion SIO_000772 18179881 NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance.
- NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_assertion wasDerivedFrom befree-2016 NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance.
- NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_assertion wasGeneratedBy ECO_0000203 NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance.
- befree-2016 importedOn "2016-02-19" NP648706.RApYvVsygCuLeE9pFOXlyClw3s5gmPueoaNx4e1IY9Mrc130_provenance.