Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance.
- NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_assertion description "[Screening for C677T and A1298C MTHFR polymorphisms in patients with epilepsy and risk of hyperhomocysteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance.
- NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_assertion evidence source_evidence_literature NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance.
- NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_assertion SIO_000772 15970629 NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance.
- NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_assertion wasDerivedFrom befree-2016 NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance.
- NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_assertion wasGeneratedBy ECO_0000203 NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance.
- befree-2016 importedOn "2016-02-19" NP500453.RAJEaHM00C4mjap9s99BT4H8GJLThOaTJlLYoUDqRtTtw130_provenance.