@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:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_head { this: np:hasAssertion dgn-np:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_assertion; np:hasProvenance dgn-np:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_provenance; np:hasPublicationInfo dgn-np:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_publicationInfo; a np:Nanopublication . dgn-np:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_assertion a np:Assertion . dgn-np:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_provenance a np:Provenance . dgn-np:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_publicationInfo a np:PublicationInfo . } dgn-np:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_assertion { miriam-gene:2944 a ncit:C16612 . lld:C0848332 a ncit:C7057 . dgn-gda:DGN5ce607bb14f99be9bf61290030ab4475 sio:SIO_000628 miriam-gene:2944, lld:C0848332; a sio:SIO_001121 . } dgn-np:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_provenance { dgn-np:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_assertion dcterms:description "[Genotyping for glutathione S-transferase micro1 (GSTM1), glutathione S-transferase theta1 (GSTT1), myeloperoxidase (MPO) (C(-)463T), nicotinamide adenine dinucleotide phosphate:quinone oxidoreductase (NQO1) (C609T), 5,10-methylenetetrahydrofolate reductase (MTHFR) (C677T), MTHFR (A1298C), methionine synthase reductase (MTRR) (A66G), X-ray repair cross complementing 1 (XRCC1) 194 (Arg194Trp), XRCC1 280 (Arg280His), and XRCC1 399 (Arg399Gln) alleles was performed by TaqMan analysis using DNA isolated from newborn heel-stick spots provided by the Minnesota Department of Health.]. 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:14716779; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP938079.RAI-v7vQD7SF5tIv9Dsp4k4ORZAECVMiCLG1f-BYZ5v9U130_publicationInfo { this: dcterms:created "2014-10-02T12:41:35+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }