Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance.
- NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_assertion description "[The combined analyses identified significant (P < 5.0 10(-8)) associations between NOA risk and common variants near PRMT6 (rs12097821 at 1p13.3: odds ratio (OR) = 1.25, P = 5.7 10(-10)), PEX10 (rs2477686 at 1p36.32: OR = 1.39, P = 5.7 10(-12)) and SOX5 (rs10842262 at 12p12.1: OR = 1.23, P = 2.3 10(-9)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance.
- NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_assertion evidence source_evidence_literature NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance.
- NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_assertion SIO_000772 22197933 NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance.
- NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_assertion wasDerivedFrom gad-20130706 NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance.
- NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_assertion wasGeneratedBy ECO_0000203 NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP96721.RA9xxQcE7gpge7GwdWeCXrDamDQRqSB-FlH1QsTt1PuFU130_provenance.