Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance.
- NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_assertion description "[Mutations in the human RDS gene are responsible for several forms of inherited blindness including autosomal-dominant retinitis pigmentosa and macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance.
- NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_assertion evidence source_evidence_literature NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance.
- NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_assertion SIO_000772 10704489 NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance.
- NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_assertion wasDerivedFrom befree-2016 NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance.
- NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_assertion wasGeneratedBy ECO_0000203 NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance.
- befree-2016 importedOn "2016-02-19" NP277192.RA4KNaZqDpmsuFt7cHlJuCRrTFGE_o1Zo8-fPKPD5m7GY130_provenance.