Matches in Nanopublications for { ?s ?p "[Hexanucleotide repeat expansions of C9orf72 are the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Hexanucleotide repeat expansions of C9orf72 are the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_assertion description "[Hexanucleotide repeat expansions of C9orf72 are the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.