Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance.
- NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_assertion description "[In contrast to UBB+1 transcripts, UBB+1 protein accumulation in the ubiquitin-containing neuropathological hallmarks is restricted to the tauopathies such as Pick disease, frontotemporal dementia, progressive supranuclear palsy, and argyrophilic grain disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance.
- NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_assertion evidence source_evidence_literature NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance.
- NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_assertion SIO_000772 14597671 NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance.
- NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_assertion wasDerivedFrom befree-2016 NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance.
- NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_assertion wasGeneratedBy ECO_0000203 NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance.
- befree-2016 importedOn "2016-02-19" NP419139.RAJxOiH1U0Owk3Q1ADDV59wiGOceV7rc_13dVSuqMhIT4130_provenance.