Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance.
- NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_assertion description "[Pathogenic mutations in APP, PSEN1, PSEN2, MAPT and GRN have previously been linked to familial early onset forms of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance.
- NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_assertion evidence source_evidence_literature NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance.
- NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_assertion SIO_000772 22312439 NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance.
- NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_assertion wasDerivedFrom befree-2016 NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance.
- NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_assertion wasGeneratedBy ECO_0000203 NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance.
- befree-2016 importedOn "2016-02-19" NP959195.RAgfK7tF-oX2_ljga7d6qF-1eYI4QSsyb0lc_jlGQoZSE130_provenance.