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- source_evidence_literature type ECO_0000212 NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_provenance.
- NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_assertion description "[However, in primiparous patients, the frequency was significantly different in elderly pregnancy (63% in severe HP vs. 18% in controls; P < 0.05), in the subgroup with the MM+MT genotypes of the angiotensinogen gene (50% in severe HP vs. 26% in controls; P < 0.05), and in the subgroup with the GA+AA genotypes of the endothelial nitric oxide synthase gene (42% in severe HP vs. 13% in controls; P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_provenance.
- NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_assertion evidence source_evidence_literature NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_provenance.
- NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_assertion SIO_000772 14719182 NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_provenance.
- NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_assertion wasDerivedFrom befree-20150227 NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_provenance.
- NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_assertion wasGeneratedBy ECO_0000203 NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP229574.RAREeheRYVVjV5E_wix21NP1i6jtgTfV9HrYBZlAo71LQ130_provenance.