Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance.
- NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_assertion description "[These findings demonstrate that both retinitis pigmentosa and macular dystrophies are caused by mutations in RDS and that the functional significance of certain amino-acids in peripherin-RDS may be different in cones and rods.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance.
- NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_assertion evidence source_evidence_literature NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance.
- NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_assertion SIO_000772 8485576 NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance.
- NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_assertion wasDerivedFrom befree-20140225 NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance.
- NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_assertion wasGeneratedBy ECO_0000203 NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP208703.RAjBOGrnppnqzqhahwHefYEY6tyRzQwDolcEWG23gACtA130_provenance.