Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance.
- NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_assertion description "[In conclusion, MTRR 66 GG and TC 776 GG genotypes in mothers and children may contribute to the risk of CHDs, particularly when the maternal vitamin B12 status is low.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance.
- NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_assertion evidence source_evidence_literature NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance.
- NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_assertion SIO_000772 18226574 NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance.
- NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_assertion wasDerivedFrom befree-20140225 NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance.
- NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_assertion wasGeneratedBy ECO_0000203 NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP540145.RACl1EfSgxJ-nGxW_gU-kNxnJ2t8BHEulqcvpaCybkLXU130_provenance.