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- source_evidence_literature type ECO_0000212 NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_provenance.
- NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_assertion description "[In conclusion, the data reported provide novel clues into molecular pathophysiological mechanisms of CLN6-deficiency, and may also help in developing disease biomarkers and therapies for this and other neurodegenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_provenance.
- NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_assertion evidence source_evidence_literature NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_provenance.
- NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_assertion SIO_000772 16857350 NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_provenance.
- NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_assertion wasDerivedFrom befree-20150227 NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_provenance.
- NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_assertion wasGeneratedBy ECO_0000203 NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_provenance.
- befree-20150227 importedOn "2015-02-27" NP915731.RAXiHHfD3khBg-ES34gDM3uLpLQ25l1VWbIqa8UGysOec130_provenance.