Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance.
- NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_assertion description "[In 158 mothers with a CHD-affected child, the maternal MTHFR 677CT and TT genotypes in combination with no use of periconceptional folate supplements were associated with, respectively, a three-fold (OR 3.3 95% CI 1.46-7.32) and six-fold (OR 6.3 95% CI 2.32-17.27) increased risk for conotruncal heart defects in offspring.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance.
- NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_assertion evidence source_evidence_literature NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance.
- NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_assertion SIO_000772 16524890 NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance.
- NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_assertion wasDerivedFrom befree-20140225 NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance.
- NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_assertion wasGeneratedBy ECO_0000203 NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance.
- befree-20140225 importedOn "2014-02-25" NP876559.RA4VLj9WQQ6uflC1-n4RHNspMpT9jmdyDzOib_wtGKg28130_provenance.