Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance.
- NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_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." NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance.
- NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_assertion evidence source_evidence_literature NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance.
- NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_assertion SIO_000772 17917582 NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance.
- NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_assertion wasDerivedFrom befree-20150227 NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance.
- NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_assertion wasGeneratedBy ECO_0000203 NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP872894.RAxhWMfuEMrYGHGbc80OjDKz9ehVBM-kPRBUBpUYxj8Oc130_provenance.