Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance.
- NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_assertion description "[genetic variants investigated in this study may be associated with a moderate modification of the risk for AD in some samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance.
- NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_assertion evidence source_evidence_literature NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance.
- NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_assertion SIO_000772 17387528 NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance.
- NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_assertion wasDerivedFrom gad-20130706 NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance.
- NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_assertion wasGeneratedBy ECO_0000203 NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance.
- gad-20130706 importedOn "2013-07-06" NP64563.RA8UiMnKFJRzKv8A2E8eiT2a1X_-YEitv0ijycwhysV_8130_provenance.