Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_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." NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion evidence source_evidence_literature NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion SIO_000772 17904392 NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion wasDerivedFrom gad-20130706 NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion wasGeneratedBy ECO_0000203 NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- gad-20130706 importedOn "2013-07-06" NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.