Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance.
- NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_assertion description "[To investigate this further, a new cohort of women with epilepsy has been identified from maternity hospital records and genotyped for polymorphisms in MTHFR, serine hydroxymethyl transferase (SHMT1), methionine synthase (MTR) and methionine synthase reductase (MTRR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance.
- NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_assertion evidence source_evidence_literature NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance.
- NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_assertion SIO_000772 17904392 NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance.
- NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_assertion wasDerivedFrom befree-20140225 NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance.
- NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_assertion wasGeneratedBy ECO_0000203 NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP295333.RAMAKXvfKy3F4JJyeUFbIVmAj9aGbqDaAvUOVfpAj1FZc130_provenance.