Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance.
- NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_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." NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance.
- NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_assertion evidence source_evidence_literature NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance.
- NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_assertion SIO_000772 11447843 NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance.
- NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_assertion wasDerivedFrom befree-20140225 NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance.
- NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_assertion wasGeneratedBy ECO_0000203 NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance.
- befree-20140225 importedOn "2014-02-25" NP313150.RAwnCWQRm0JVkPv2FlKf1zAeei0DEb4tHvTEb0cusboko130_provenance.