Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance.
- NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_assertion description "[In addition, UBB+1, a mutant form of ubiquitin and a marker for proteasomal dysfunction, was present in the majority of NFTs, whereas co-existence of alpha-synuclein and UBB+1 was found in only a few neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance.
- NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_assertion evidence source_evidence_literature NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance.
- NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_assertion SIO_000772 17237936 NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance.
- NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_assertion wasDerivedFrom befree-20140225 NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance.
- NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_assertion wasGeneratedBy ECO_0000203 NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP620795.RAILk8yvXdeevh-dD190O2K_5hoPi07ijSvuqD3BT3zg4130_provenance.