Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance.
- NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_assertion description "[Our study suggests that both C677T and A1298C MTHFR polymorphisms should be examined when assessing genetic risk factors of hyperhomocysteinemia in epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance.
- NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_assertion evidence source_evidence_literature NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance.
- NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_assertion SIO_000772 15970629 NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance.
- NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_assertion wasDerivedFrom befree-20140225 NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance.
- NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_assertion wasGeneratedBy ECO_0000203 NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP480954.RAYoGHD_HN0FsXFiwzHeL_DsXBAwJCfCBxBcvDAn5YLy0130_provenance.