Matches in Nanopublications for { ?s ?p "[The GGGGCC hexanucleotide expansion in the C9ORF72 gene is the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion description "[The GGGGCC hexanucleotide expansion in the C9ORF72 gene is the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_assertion description "[The GGGGCC hexanucleotide expansion in the C9ORF72 gene is the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244135.RAfb8YjfrtEdDC_Sa6_-NK9eYRDzz9xYoeCT8-af8E9gY130_provenance.
- NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_assertion description "[The GGGGCC hexanucleotide expansion in the C9ORF72 gene is the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244138.RAQBjmpc0qt027TOx5duPaIIUh5Lxa40HK-y3g0oFmKMU130_provenance.
- NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_assertion description "[The GGGGCC hexanucleotide expansion in the C9ORF72 gene is the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244140.RAahKjBX2SjwSA4gsq442B6Fx8M5cUJ3ev0MXDcgr1N4E130_provenance.
- NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_assertion description "[The GGGGCC hexanucleotide expansion in the C9ORF72 gene is the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244143.RAYfnIHw8MekkFlS7pH7Go5C9kXYeMZoxfz4yj4zjITQ4130_provenance.