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- source_evidence_literature type ECO_0000212 NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_provenance.
- NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_assertion description "[These latter proteins include the ABri and ADan subunits in familial British dementia and familial Danish dementia, respectively, which are also known under the umbrella term BRI2 gene-related dementias, variant cystatin C in hereditary cerebral haemorrhage with amyloidosis of Icelandic-type, variant transthyretins in meningo-vascular amyloidosis, disease-associated prion protein (PrP(Sc)) in hereditary prion disease with premature stop codon mutations and mutated gelsolin (AGel) in familial amyloidosis of Finnish type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_provenance.
- NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_assertion evidence source_evidence_literature NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_provenance.
- NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_assertion SIO_000772 19225789 NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_provenance.
- NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_assertion wasDerivedFrom befree-2016 NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_provenance.
- NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_assertion wasGeneratedBy ECO_0000203 NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_provenance.
- befree-2016 importedOn "2016-02-19" NP721279.RACJA_A1Ekh42yQhZpSGfZcouZ75472WQA3Hgt49xihNA130_provenance.