Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance.
- NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_assertion description "[WG patients without ESRD had a higher frequency of the IL10 GCC/ACC promotor genotype (OR = 0.13) and long CTLA4 (AT)(n) repeats (OR = 0.4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance.
- NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_assertion evidence source_evidence_literature NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance.
- NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_assertion SIO_000772 15708894 NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance.
- NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_assertion wasDerivedFrom befree-20150227 NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance.
- NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_assertion wasGeneratedBy ECO_0000203 NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP830508.RAiHxUNrDLeks9u6gdfVsGiCjjX_Chr28_c0E1GE4uyKA130_provenance.