Matches in Nanopublications for { ?s ?p "[Mutations in C9ORF72, SOD1, TARDBP, and FUS genes account for approximately two-third of familial cases and 5% of sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_assertion description "[Mutations in C9ORF72, SOD1, TARDBP, and FUS genes account for approximately two-third of familial cases and 5% of sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.
- NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_assertion description "[Mutations in C9ORF72, SOD1, TARDBP, and FUS genes account for approximately two-third of familial cases and 5% of sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_provenance.
- assertion description "[Mutations in C9ORF72, SOD1, TARDBP, and FUS genes account for approximately two-third of familial cases and 5% of sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1146038.RARqN3cmihHDQcdROfXG55RQvdcpkIOjwzPGrINX4d9VU130_assertion description "[Mutations in C9ORF72, SOD1, TARDBP, and FUS genes account for approximately two-third of familial cases and 5% of sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1146038.RARqN3cmihHDQcdROfXG55RQvdcpkIOjwzPGrINX4d9VU130_provenance.
- NP1146039.RAUwC7nk4yEZYbHmqRdtuQf1o7uYZWGyx_l775ni4h-tE130_assertion description "[Mutations in C9ORF72, SOD1, TARDBP, and FUS genes account for approximately two-third of familial cases and 5% of sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1146039.RAUwC7nk4yEZYbHmqRdtuQf1o7uYZWGyx_l775ni4h-tE130_provenance.
- assertion description "[Mutations in C9ORF72, SOD1, TARDBP, and FUS genes account for approximately two-third of familial cases and 5% of sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.