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- NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_assertion type Assertion NP218207.RAV69xI9N-g2g2NMtJqkMAT7UAl5f_IqJhBt0YWO4GGG4130_head.
- 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.