Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance.
- NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_assertion description "[Specifically, we will discuss how pathologies linked to the Dutch (E693Q) and Flemish AbetaPP (A692G) mutations have helped in understanding the role of CAA in dementia and in the development of dense-core plaques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance.
- NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_assertion evidence source_evidence_literature NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance.
- NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_assertion SIO_000772 16914877 NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance.
- NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_assertion wasDerivedFrom befree-2016 NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance.
- NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_assertion wasGeneratedBy ECO_0000203 NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance.
- befree-2016 importedOn "2016-02-19" NP564687.RACXjdHpoBedcLYlIy90GTvW9uNMlax2XI20WrMlwRCVo130_provenance.