Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance.
- NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_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." NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance.
- NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_assertion evidence source_evidence_literature NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance.
- NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_assertion SIO_000772 18226574 NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance.
- NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_assertion wasDerivedFrom gad-20150221 NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance.
- NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_assertion wasGeneratedBy ECO_0000203 NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP91188.RA6png4oa23y7YDaeSnE8gRNDEahd8eFzBz8KdiiA_Dqg130_provenance.