Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance.
- NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_assertion description "[GSTT1 null genotype was associated with 2.23-fold (p < 0.05) increased risk for HCC development as compared to the control group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance.
- NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_assertion evidence source_evidence_literature NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance.
- NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_assertion SIO_000772 18816171 NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance.
- NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_assertion wasDerivedFrom befree-2016 NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance.
- NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_assertion wasGeneratedBy ECO_0000203 NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance.
- befree-2016 importedOn "2016-02-19" NP694906.RAE9D43aN5QkXaLqjNDWpc3x-Qc4qMdAgssgvr-ANhDRY130_provenance.