Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance.
- NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_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." NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance.
- NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_assertion evidence source_evidence_literature NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance.
- NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_assertion SIO_000772 17904392 NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance.
- NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_assertion wasDerivedFrom befree-20140225 NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance.
- NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_assertion wasGeneratedBy ECO_0000203 NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP602645.RA0oQblw7JyWVUdFkKsiRGm0Wa0B3ZUjtSUFBz-nWihBc130_provenance.