@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_head {
   this: np:hasAssertion dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_assertion ;
    np:hasProvenance dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_provenance ;
    np:hasPublicationInfo dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_assertion a np:Assertion .
  dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_provenance a np:Provenance .
  dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_assertion {
   miriam-gene:4548 a ncit:C16612 .
  lld:C0025286 a ncit:C7057 .
  dgn-gda:DGNc66fd60f71e8ec591bc6d5947d68a23f sio:SIO_000628 miriam-gene:4548 , lld:C0025286 ;
    a sio:SIO_001122 .
}
dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_provenance {
   dgn-np:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_assertion dcterms:description "[To test the hypothesis that polymorphic variation in the folate metabolism genes 5,10-methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTRR), and methionine synthase reductase (MTR) influences the risk of primary brain tumors, we genotyped 1,005 glioma cases, 631 meningioma cases, and 1,101 controls for the MTHFR C677A and A1298C, MTRR A66G, and MTR A2756G variants.]. 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:18483342 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP123121.RAf5vJij9K-pe7tQjufltNbFguQ4Z0hlmH2UujC4QeqGw130_publicationInfo {
   this: dcterms:created "2016-05-13T12:42:43+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}