Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_assertion> ?p ?o ?g. }
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- NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_assertion type Assertion NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_head.
- NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_assertion description "[Autosomal dominant early-onset Alzheimer disease (EOAD) is a heterogeneous condition that has been associated with mutations in 3 different genes: the amyloid precursor protein (APP), presenilin 1 (PSEN1), and presenilin 2 (PSEN2) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_provenance.
- NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_assertion evidence source_evidence_literature NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_provenance.
- NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_assertion SIO_000772 19073399 NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_provenance.
- NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_assertion wasDerivedFrom befree-20150227 NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_provenance.
- NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_assertion wasGeneratedBy ECO_0000203 NP650838.RAgUj8zfSDwtN2HPzUC6VS-nSyc2N0Y-fzu45ESqAAZZg130_provenance.