Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_assertion> ?p ?o ?g. }
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- NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_assertion type Assertion NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_head.
- NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_assertion description "[A total of 76 subjects, including 56 with a clinical diagnosis of behavioural variant frontotemporal dementia and a mutation in one of these genes (19 with C9ORF72 mutations, 25 with tau mutations and 12 with progranulin mutations) and 20 sporadic subjects with behavioural variant frontotemporal dementia (including 50% with amyotrophic lateral sclerosis), with magnetic resonance imaging were included in this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_provenance.
- NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_assertion evidence source_evidence_literature NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_provenance.
- NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_assertion SIO_000772 22366795 NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_provenance.
- NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_assertion wasDerivedFrom befree-2016 NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_provenance.
- NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_assertion wasGeneratedBy ECO_0000203 NP963486.RA819V6i9Q4DBeRd9qUkW9ZdLksUCN-c-LvSgnxKXT6uk130_provenance.