Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_assertion> ?p ?o ?g. }
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- NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_assertion type Assertion NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_head.
- NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_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." NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance.
- NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_assertion evidence source_evidence_literature NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance.
- NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_assertion SIO_000772 19073399 NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance.
- NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_assertion wasDerivedFrom befree-2016 NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance.
- NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_assertion wasGeneratedBy ECO_0000203 NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance.