Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance.
- NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_assertion wasGeneratedBy ECO_0000203 NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance.
- NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_assertion wasDerivedFrom befree-20150227 NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance.
- NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_assertion SIO_000772 15541726 NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance.
- NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_assertion evidence source_evidence_literature NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance.
- NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_assertion description "[PAP-1 has been identified by us as a Pim-1-binding protein and has recently been implicated as the defective gene in RP9, one type of autosomal dominant retinitis pigmentosa (adRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869682.RAnFcEf03Bjdg8iV_MrVDIRwEmc2Gc5eVN6N5xAE3W-0A130_provenance.