Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance.
- NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_assertion description "[Association between the SCGB3A2 rs1368408 SNP and GD was detected (p = 0.007, odds ratio = 1.18, 95% confidence intervals = 1.05-1.33).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance.
- NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_assertion evidence source_evidence_literature NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance.
- NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_assertion SIO_000772 20210668 NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance.
- NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_assertion wasDerivedFrom befree-20150227 NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance.
- NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_assertion wasGeneratedBy ECO_0000203 NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP966592.RAZseGVfH_q6VYi94m1P-LZFTXz5jGI65tUc3Xibr4WsQ130_provenance.