Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance.
- NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_assertion description "[For all patients, the rs12980275 A allele increased the odds for significant fibrosis (F ? 2) odds ratio (OR) = 1.68; p = 0.018) and more rapid fibrosis progression (FPR ? 0.075 fibrosis units/year) (OR = 1.64; p = 0.035), and decreased the odds for liver steatosis (OR = 0.61; p = 0.046).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance.
- NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_assertion evidence source_evidence_literature NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance.
- NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_assertion SIO_000772 23103287 NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance.
- NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_assertion wasDerivedFrom befree-2016 NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance.
- NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_assertion wasGeneratedBy ECO_0000203 NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1024187.RAEC10f3VkVd3ovKLPHZugY2Ci9otx98mlr7bWXtj0D-I130_provenance.