Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance.
- NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_assertion description "[In conclusion, the presence of three or more polymorphic alleles for MTHFR C677T, MTHFR A1298C, MTR A2756G, and RFC1 A80G, and plasma Hcy concentrations higher than 4.99 micromol/L are maternal risk factors for DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance.
- NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_assertion evidence source_evidence_literature NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance.
- NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_assertion SIO_000772 18273817 NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance.
- NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_assertion wasDerivedFrom gad-20150221 NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance.
- NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_assertion wasGeneratedBy ECO_0000203 NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP79396.RAFTHsExpzLcuUaexQGvYba4sA6yhMfHZx3RhAR1OTFlw130_provenance.