Matches in Nanopublications for { ?s ?p "[The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_assertion description "[The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705756.RAsIFZZIomzFW3PeGuQF3ytuw0w-2GiEMXHX2euPLwGAM130_provenance.
- NP407300.RAPkznxyrcEBGVAJEHos770cEBgS_m7fm5z2_UOFNgdgg130_assertion description "[The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP407300.RAPkznxyrcEBGVAJEHos770cEBgS_m7fm5z2_UOFNgdgg130_provenance.
- assertion description "[The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_assertion description "[The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_provenance.
- NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_assertion description "[The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958163.RAw7GW3fxeihLY34kFICp-u7HkLS26VXEgM-BNlfCqSOA130_provenance.