Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance.
- NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_assertion description "[This is the first published case with the fully developed clinical and neuroimaging picture of posterior cortical atrophy, morphologically presenting as a distinct phenotype of 4R-tauopathy that closely resembles (atypical) CBD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance.
- NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_assertion evidence source_evidence_literature NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance.
- NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_assertion SIO_000772 20571819 NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance.
- NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_assertion wasDerivedFrom befree-20140225 NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance.
- NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_assertion wasGeneratedBy ECO_0000203 NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP210211.RAX2IrF2s7WL3M3Hhpwxbk2KQxUvtNlwxXgfY3NiJ1qHY130_provenance.