Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance.
- NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_assertion description "[The combined analyses identified significant (P < 5.0 A 10(-8)) associations between NOA risk and common variants near PRMT6 (rs12097821 at 1p13.3: odds ratio (OR) = 1.25, P = 5.7 A 10(-10)), PEX10 (rs2477686 at 1p36.32: OR = 1.39, P = 5.7 A 10(-12)) and SOX5 (rs10842262 at 12p12.1: OR = 1.23, P = 2.3 A 10(-9)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance.
- NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_assertion evidence source_evidence_literature NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance.
- NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_assertion SIO_000772 22197933 NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance.
- NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_assertion wasDerivedFrom gad-20150221 NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance.
- NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_assertion wasGeneratedBy ECO_0000203 NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP159994.RAv5KTqXo3E_P7ATMZTooYX3QBUWntwxkeGdtPsa6pNGE130_provenance.