@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_head { this: np:hasAssertion dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_assertion; np:hasProvenance dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_provenance; np:hasPublicationInfo dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_publicationInfo; a np:Nanopublication . dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_assertion a np:Assertion . dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_provenance a np:Provenance . dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_publicationInfo a np:PublicationInfo . } dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_assertion { miriam-gene:4524 a ncit:C16612 . lld:C0014544 a ncit:C7057 . dgn-gda:DGN8c1383ede3d6860ee4d45dd7bad3fd35 sio:SIO_000628 miriam-gene:4524, lld:C0014544; a sio:SIO_001122 . } dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_provenance { dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_assertion dcterms:description "[The purpose of the study was to determine the frequency of occurrence of polymorphisms of genes MTHFR (C677T), MTR (A2756G), and MTHFD1 (G1958A), as well as to analyze the concentration of homocysteine (Hcy), methionine (Met), asymmetric dimethylarginine (ADMA), and arginine (Arg) in epileptics treatment with antiepileptic drugs (AEDs), and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:21543238; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP891730.RAnyjypQ85rQC98BQ1h25GVfyutrDCbXYYFjG1JWuQ2jg130_publicationInfo { this: dcterms:created "2016-05-13T12:48:28+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }