Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance.
- NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_assertion description "[CALHM1 gene coding non-synonymous SNP P86L (rs2986017) was reported to increase the risk of Alzheimer's disease (AD) in a recent study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance.
- NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_assertion evidence source_evidence_literature NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance.
- NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_assertion SIO_000772 20164592 NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance.
- NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_assertion wasDerivedFrom befree-20140225 NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance.
- NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_assertion wasGeneratedBy ECO_0000203 NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP785159.RAgSIDWXPm92G_q44YyusQzQsJO54XWx_C_07hJZrepwk130_provenance.