Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance.
- NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_assertion description "[Additionally, systematic review and meta-analysis of the literature for genetic association studies of D2 Thr92Ala polymorphism and DM2 were performed in Medline, Embase, LiLacs, and SciELO, and major meeting databases using the terms 'rs225014' odds ratio (OR) 'thr92ala' OR 'T92A' OR 'dio2 a/g'.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance.
- NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_assertion evidence source_evidence_literature NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance.
- NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_assertion SIO_000772 20566590 NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance.
- NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_assertion wasDerivedFrom gad-20150221 NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance.
- NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_assertion wasGeneratedBy ECO_0000203 NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP179090.RAUxx2Hy0F8_pliVWmq_Dgexk9vCmokF2poAWS0H0wASw130_provenance.