Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance.
- NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_assertion description "[An earlier age at onset has also been demonstrated in familial AD patients with mutations in the amyloid precursor protein (APP) gene (APP717 and APP670/671)13 carrying the APOE epsilon-4 allele compared to those who do not, but not in familial AD patients with APP692 or 693 mutations, or in chromosome 14-linked familial AD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance.
- NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_assertion evidence source_evidence_literature NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance.
- NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_assertion SIO_000772 7550352 NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance.
- NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_assertion wasDerivedFrom befree-2016 NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance.
- NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_assertion wasGeneratedBy ECO_0000203 NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1312192.RA14y6DIFkQGF-Cs9fHx77_X2IN4-Sy4HprUBdwOOpH5U130_provenance.