Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance.
- NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_assertion description "[In addition, mutations in glycine-N-methyltransferase (GNMT) could be associated with a higher risk of hepatocellular carcinoma and liver disease due to an unbalanced S-adenosylmethionine (SAM)/S-adenosylhomocysteine (SAH) ratio, which leads to aberrant methylation reactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance.
- NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_assertion evidence source_evidence_literature NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance.
- NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_assertion SIO_000772 23474979 NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance.
- NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_assertion wasDerivedFrom befree-2016 NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance.
- NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_assertion wasGeneratedBy ECO_0000203 NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1059228.RAGyJn_0Ud-yMGl3lYQbvpyt53Sbbvyw5pFIXNqqp0Vi0130_provenance.