Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance.
- NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_assertion description "[Since the presence of the rs2304052 C allele is associated with an increased risk (odds ratio: 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance.
- NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_assertion evidence source_evidence_literature NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance.
- NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_assertion SIO_000772 19817957 NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance.
- NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_assertion wasDerivedFrom gad-20130706 NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance.
- NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_assertion wasGeneratedBy ECO_0000203 NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP78711.RADd00RePROyy1vbUnWubx0WiIHS7pQQz6YLSa0hCslKk130_provenance.