Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP708413.RAHDvLhSBJGtYfDGzglKK4qzxPXt0tGt8EKVBfJKOg2Fs130_provenance.