Matches in Nanopublications for { ?s ?p "[The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of sporadic and familial forms of amyotrophic lateral sclerosis and frontotemporal dementia.The basis for pathogenesis is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of sporadic and familial forms of amyotrophic lateral sclerosis and frontotemporal dementia.The basis for pathogenesis is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of sporadic and familial forms of amyotrophic lateral sclerosis and frontotemporal dementia.The basis for pathogenesis is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of sporadic and familial forms of amyotrophic lateral sclerosis and frontotemporal dementia.The basis for pathogenesis is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_assertion description "[The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of sporadic and familial forms of amyotrophic lateral sclerosis and frontotemporal dementia.The basis for pathogenesis is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293228.RAO3V2JGr3t8JVW2giUwAQ1r5p54duP4wC-tCh8affLO4130_provenance.
- NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_assertion description "[The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of sporadic and familial forms of amyotrophic lateral sclerosis and frontotemporal dementia.The basis for pathogenesis is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293227.RA4MWONzChNYpYTMbsSh3HRNlSNo2Xvuj_lc3TiCuwUR4130_provenance.
- NP1293229.RA-w8lbd7oV1QlJ2JS7shArg45tIB22BYzs6pBCNB-P-A130_assertion description "[The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of sporadic and familial forms of amyotrophic lateral sclerosis and frontotemporal dementia.The basis for pathogenesis is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293229.RA-w8lbd7oV1QlJ2JS7shArg45tIB22BYzs6pBCNB-P-A130_provenance.