Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
Showing items 1 to 7 of
7
with 100 items per page.
- 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.
- 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." provenance.
- 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." provenance.
- 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." provenance.
- NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_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." NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.
- NP626375.RAoPlGMJpBu3ue4dkDuyySJWUFwA9K8j5Pod5qsz9fa6I130_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." NP626375.RAoPlGMJpBu3ue4dkDuyySJWUFwA9K8j5Pod5qsz9fa6I130_provenance.
- NP626377.RAqV_1E3zYKSzCapVOGPUOOJ3MYRlJ2ykzeQJ3s3GkYJA130_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." NP626377.RAqV_1E3zYKSzCapVOGPUOOJ3MYRlJ2ykzeQJ3s3GkYJA130_provenance.