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- source_evidence_literature type ECO_0000212 NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_provenance.
- NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_assertion description "[Neuropathological examination in six cases with C9ORF72 mutation from the frontotemporal lobar degeneration series identified histomorphological features consistent with either type A or B TAR DNA-binding protein-43 deposition; however, p62-positive (in excess of TAR DNA-binding protein-43 positive) neuronal cytoplasmic inclusions in hippocampus and cerebellum were a consistent feature of these cases, in contrast to the similar frequency of p62 and TAR DNA-binding protein-43 deposition in 53 control cases with frontotemporal lobar degeneration-TAR DNA-binding protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_provenance.
- NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_assertion evidence source_evidence_literature NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_provenance.
- NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_assertion SIO_000772 22366791 NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_provenance.
- NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_assertion wasDerivedFrom befree-2016 NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_provenance.
- NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_assertion wasGeneratedBy ECO_0000203 NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_provenance.
- befree-2016 importedOn "2016-02-19" NP963453.RAYoqbHDvSsONIqwW4VHs127-eoiFRcVqVEq1Vy9laic0130_provenance.