Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance.
- NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_assertion description "[Missense mutations in presenilin 1 (PS1) and presenilin 2 (PS2) are associated with early-onset familial Alzheimer's disease which displays an accelerated deposition of amyloid plaques and neurofibrillary tangles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance.
- NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_assertion evidence source_evidence_literature NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance.
- NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_assertion SIO_000772 11447843 NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance.
- NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_assertion wasDerivedFrom befree-20150227 NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance.
- NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_assertion wasGeneratedBy ECO_0000203 NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP651094.RAyYlXH2fLA1qG30KkPevh74EOLzM1k9OxcS59lDO94JM130_provenance.