Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance.
- NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_assertion description "[When all groups were pooled, we found an association between HSD17B1 (A variant allele vs. G wild allele: odds ratio (OR)=1.42, 95% confidence interval (CI)=1.10-1.84, P=0.007) and PR (P2 variant allele vs. P1 wild allele, OR=1.43, 95% CI=0.99-2.08, P=0.058) polymorphisms and endometriosis risk, while failing to detect links with CYP17, ER, and CYP19 polymorphisms examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance.
- NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_assertion evidence source_evidence_literature NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance.
- NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_assertion SIO_000772 22613790 NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance.
- NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_assertion wasDerivedFrom befree-2016 NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance.
- NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_assertion wasGeneratedBy ECO_0000203 NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance.
- befree-2016 importedOn "2016-02-19" NP983949.RAky5TW76FKBAapASBmvY3b9VGVgozt1jNFHWuxbI1fTU130_provenance.