Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance.
- NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_assertion description "[Neuropathological changes associated with Alzheimer's disease (AD) such as amyloidplaques, cerebral amyloid angiopathy, and related pathologies are reproduced in APP23 transgenic mice overexpressing amyloid precursor protein (APP) with the Swedish mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance.
- NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_assertion evidence source_evidence_literature NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance.
- NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_assertion SIO_000772 13679413 NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance.
- NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_assertion wasDerivedFrom befree-20140225 NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance.
- NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_assertion wasGeneratedBy ECO_0000203 NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance.