Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance.
- NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_assertion description "[In this study, NR2E3 mutations (p.G56R, p.V118M) were found to be responsible for approximately 2.9% of overall RP in Chinese patients, comparable to the contributions of RHO and RP1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance.
- NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_assertion evidence source_evidence_literature NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance.
- NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_assertion SIO_000772 19933183 NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance.
- NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_assertion wasDerivedFrom befree-20140225 NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance.
- NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_assertion wasGeneratedBy ECO_0000203 NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP629480.RAl5nF9nwfaPbL9r-cDR3R5eMCeb5YPUPJ6jylGqgER8U130_provenance.