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- source_evidence_literature type ECO_0000212 NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_provenance.
- NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_assertion description "[The mutation screening of PTPN22 in AD patients (n=332) and controls (n=112) revealed eight missense variants, five of which have not been reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_provenance.
- NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_assertion evidence source_evidence_literature NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_provenance.
- NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_assertion SIO_000772 18301444 NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_provenance.
- NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_assertion wasDerivedFrom befree-2016 NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_provenance.
- NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_assertion wasGeneratedBy ECO_0000203 NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_provenance.
- befree-2016 importedOn "2016-02-19" NP657490.RAy85Y-Dm9QVtrCJnHOY6tWh7XPT1OigSf--wfWo-reYk130_provenance.