Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance.
- NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_assertion description "[The finding of ubiquitin- and p62-positive, TDP-43-negative cytoplasmic inclusions in the hippocampus and neocortex suggests reclassification of the neuropathology of FTD-3 as a unique subtype of frontotemporal lobar degeneration with ubiquitin-positive inclusions that are TDP-43-negative.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance.
- NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_assertion evidence source_evidence_literature NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance.
- NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_assertion SIO_000772 17917582 NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance.
- NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_assertion wasDerivedFrom befree-2016 NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance.
- NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_assertion wasGeneratedBy ECO_0000203 NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance.
- befree-2016 importedOn "2016-02-19" NP633797.RA5mjMspgLaGSv5wzUGWjEPf1gTqaxUjjUB_rT8Rm5W5w130_provenance.