Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance.
- NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_assertion description "[To study the role of Abeta amyloid deposits in the generation of cytoskeletal lesions, we have generated a transgenic mouse line coexpressing in the same neurons a wild-type human tau isoform (0N3R), a mutant form of APP (751SL) and a mutant form of PS1 (M146L).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance.
- NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_assertion evidence source_evidence_literature NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance.
- NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_assertion SIO_000772 14751770 NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance.
- NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_assertion wasDerivedFrom befree-2016 NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance.
- NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_assertion wasGeneratedBy ECO_0000203 NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance.
- befree-2016 importedOn "2016-02-19" NP430030.RAYX95DLAx7g7Jv3x1JNn5fKDnCjV4HRSW7QWk1y0s-Bs130_provenance.