Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance.
- NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_assertion description "[Further, combination of GSTM1 and T1 genotypes with either of exon 3 or 4 polymorphism of mEPHX displayed synergistic associations (risk or protective) for HCC development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance.
- NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_assertion evidence source_evidence_literature NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance.
- NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_assertion SIO_000772 18816171 NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance.
- NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_assertion wasDerivedFrom befree-2016 NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance.
- NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_assertion wasGeneratedBy ECO_0000203 NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance.
- befree-2016 importedOn "2016-02-19" NP694900.RA70wFZFDXAXSZoLgfWbZIUD3S6LTobZu8-d3c1zCQ1pc130_provenance.