Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance.
- NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_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." NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance.
- NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_assertion evidence source_evidence_literature NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance.
- NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_assertion SIO_000772 17904392 NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance.
- NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_assertion wasDerivedFrom befree-20150227 NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance.
- NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_assertion wasGeneratedBy ECO_0000203 NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP577633.RASI5dttI9BjQEuC6Z8Y1bn20dDPYRrMXZG54L3JpB8z0130_provenance.