Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance.
- NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_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." NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance.
- NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_assertion evidence source_evidence_literature NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance.
- NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_assertion SIO_000772 18226574 NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance.
- NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_assertion wasDerivedFrom befree-20140225 NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance.
- NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_assertion wasGeneratedBy ECO_0000203 NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP659493.RAoHjipFr1HiMn92m6BkVFJjraW7BhFhB9kKj7mqAh_Lg130_provenance.