Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance.
- NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_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." NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance.
- NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_assertion evidence source_evidence_literature NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance.
- NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_assertion SIO_000772 18273817 NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance.
- NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_assertion wasDerivedFrom befree-20140225 NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance.
- NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_assertion wasGeneratedBy ECO_0000203 NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP696592.RApAUzsLtx2tnOKE5o0QjY6M8_AFocisCxCXe5ZWBsj4c130_provenance.