Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance.
- NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_assertion description "[We herein report the case of a German EOAD patient with a family history of dementia and a missense mutation at codon 141 (N141I) of the PSEN2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance.
- NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_assertion evidence source_evidence_literature NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance.
- NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_assertion SIO_000772 19073399 NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance.
- NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_assertion wasDerivedFrom befree-20140225 NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance.
- NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_assertion wasGeneratedBy ECO_0000203 NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212536.RAsG31WwFCyOmH3WyPluPQagz7PomWUPEh32Z9RhkgwMA130_provenance.