Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance.
- NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_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." NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance.
- NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_assertion evidence source_evidence_literature NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance.
- NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_assertion SIO_000772 17904392 NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance.
- NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_assertion wasDerivedFrom befree-2016 NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance.
- NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_assertion wasGeneratedBy ECO_0000203 NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance.
- befree-2016 importedOn "2016-02-19" NP632458.RAaHC2PsqC8M_6Way4Z7ZNGmbBxogWX0ogJPOhIFqemQo130_provenance.