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- source_evidence_literature type ECO_0000212 NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_provenance.
- NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_assertion description "[In a Belgian FTD patient series, the prevalence of PGRN mutations was 3.5 times higher than that of MAPT mutations underscoring a major role for PGRN in FTD pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_provenance.
- NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_assertion evidence source_evidence_literature NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_provenance.
- NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_assertion SIO_000772 17168647 NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_provenance.
- NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_assertion wasDerivedFrom befree-2016 NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_provenance.
- NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_assertion wasGeneratedBy ECO_0000203 NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_provenance.
- befree-2016 importedOn "2016-02-19" NP584296.RA839nrEOzHSo1Kd77fRuS4ew1aKeEze6Rzg_BB-Gdb1g130_provenance.