Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance.
- NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_assertion description "[We describe a distinct retinal disorder, autosomal-recessive bestrophinopathy (ARB), that is consequent upon biallelic mutation in BEST1 and is associated with central visual loss, a characteristic retinopathy, an absent electro-oculogram light rise, and a reduced electroretinogram.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance.
- NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_assertion evidence source_evidence_literature NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance.
- NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_assertion SIO_000772 18179881 NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance.
- NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_assertion wasDerivedFrom befree-20140225 NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance.
- NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_assertion wasGeneratedBy ECO_0000203 NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP768437.RAwkPqqzzdiQOA6vvSuUy-Z273Qj4e5l2m5pMgoE-32jU130_provenance.