Matches in Nanopublications for { ?s ?p "[Hexanucleotide repeat expansions in chromosome 9 open reading frame 72 (C9ORF72) are the most common known genetic cause of frontotemporal dementia (FTD) and motor neuron disease (MND).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_assertion description "[Hexanucleotide repeat expansions in chromosome 9 open reading frame 72 (C9ORF72) are the most common known genetic cause of frontotemporal dementia (FTD) and motor neuron disease (MND).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911555.RAbC2ZNiHGcL5Ggr4K_p9R66W9YvAPU7L5vY3UkruoZs8130_provenance.
- NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_assertion description "[Hexanucleotide repeat expansions in chromosome 9 open reading frame 72 (C9ORF72) are the most common known genetic cause of frontotemporal dementia (FTD) and motor neuron disease (MND).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108193.RASRqk5TU4tdon3hWJTkcOwMCDVXeFsjWtg23MPzPNZ3Y130_provenance.
- assertion description "[Hexanucleotide repeat expansions in chromosome 9 open reading frame 72 (C9ORF72) are the most common known genetic cause of frontotemporal dementia (FTD) and motor neuron disease (MND).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.