Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance.
- NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_assertion description "[Several other SNPs in the candidate genes, such as CTLA4, HAVCR1, and SUMO4, also had rather small p-values (<0.05), suggesting the associations between them and RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance.
- NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_assertion evidence source_evidence_literature NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance.
- NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_assertion SIO_000772 18466531 NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance.
- NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_assertion wasDerivedFrom gad-20150221 NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance.
- NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_assertion wasGeneratedBy ECO_0000203 NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP116059.RAdnHdxufFCvBWTW5IWeLigZ0kvJ_Ww2yA_MPKbfreTBo130_provenance.