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- source_evidence_literature type ECO_0000212 NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_provenance.
- NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_assertion wasGeneratedBy ECO_0000203 NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_provenance.
- NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_assertion wasDerivedFrom befree-20140225 NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_provenance.
- NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_assertion SIO_000772 17715352 NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_provenance.
- NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_assertion evidence source_evidence_literature NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_provenance.
- NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_assertion description "[TAU gene mutations that alter the inclusion of exon 10, and hence the 4R:3R ratio, are causal in the tauopathy frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_provenance.