Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance.
- NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_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." NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance.
- NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_assertion evidence source_evidence_literature NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance.
- NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_assertion SIO_000772 18816171 NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance.
- NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_assertion wasDerivedFrom gad-20150221 NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance.
- NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_assertion wasGeneratedBy ECO_0000203 NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP51023.RA4UHkxeodI7xgni9IXqtjG8_R6_YwdDuXmzt850PWtGQ130_provenance.