Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance.
- NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_assertion description "[Rare mutations in the gene encoding for tau (MAPT, microtubule-associated protein tau) cause frontotemporal dementia-spectrum (FTD-s) disorders, including FTD, progressive supranuclear palsy (PSP) and corticobasal syndrome, and a common extended haplotype spanning across the MAPT locus is associated with increased risk of PSP and Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance.
- NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_assertion evidence source_evidence_literature NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance.
- NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_assertion SIO_000772 22556362 NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance.
- NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_assertion wasDerivedFrom befree-20150227 NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance.
- NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_assertion wasGeneratedBy ECO_0000203 NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP546061.RALXMWMx4XdNF4hSMJXqRxxO1MS6ZwR5lqiwdX7Fh5PYY130_provenance.