Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance.
- NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_assertion description "[The overall results suggest that there may be a small excess risk of HCC in individuals with GSTT1 null and possibly also with GSTM1 null genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance.
- NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_assertion evidence source_evidence_literature NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance.
- NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_assertion SIO_000772 18065725 NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance.
- NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_assertion wasDerivedFrom gad-20150221 NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance.
- NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_assertion wasGeneratedBy ECO_0000203 NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP116135.RAa1J5wVkNg-np0Y9IdM2mimxdy7Y0MLxTL8Yq63XLdIs130_provenance.