Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_assertion type Assertion NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_head.
- NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_assertion wasGeneratedBy ECO_0000203 NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_provenance.
- NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_assertion wasDerivedFrom befree-2016 NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_provenance.
- NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_assertion SIO_000772 10412802 NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_provenance.
- NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_assertion evidence source_evidence_literature NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_provenance.
- NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_assertion description "[Recently intronic and exonic mutations in the Tau gene have been found to be associated with familial neurodegenerative syndromes characterized not only by a predominantly frontotemporal dementia but also by the presence of neurological signs consistent with the dysfunction of multiple subcortical neuronal circuitries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258123.RAGHtmD7FjGFzuls41aLKV-Es4dd1-osFK5uT8yP_jnWk130_provenance.