Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance.
- NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_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." NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance.
- NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_assertion evidence source_evidence_literature NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance.
- NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_assertion SIO_000772 18226574 NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance.
- NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_assertion wasDerivedFrom befree-2016 NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance.
- NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_assertion wasGeneratedBy ECO_0000203 NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance.
- befree-2016 importedOn "2016-02-19" NP652224.RAF0mpChkC12x0Mi2Wk8lw1aiMWh9d1bVA3vPY2sTcnfg130_provenance.