@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8> .
@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:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_head {
  this: np:hasAssertion dgn-np:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_assertion ;
    np:hasProvenance dgn-np:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_provenance ;
    np:hasPublicationInfo dgn-np:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_assertion a np:Assertion .
  dgn-np:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_provenance a np:Provenance .
  dgn-np:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_assertion {
  miriam-gene:57026 a ncit:C16612 .
  lld:C0349459 a ncit:C7057 .
  dgn-gda:DGN38d509ba739a9e1fb9d5772bdce8e742 sio:SIO_000628 miriam-gene:57026 , lld:C0349459 ;
    a sio:SIO_001122 .
}
dgn-np:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_provenance {
  dgn-np:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_assertion dcterms:description "[The current study investigated the following in a FA fortified population: 1) The association between MTHFR C677T polymorphism and risk of CIN 2+; 2) The modifying effects of plasma folate concentrations on this association; and 3) The modifying effects of plasma folate on the association between the polymorphism and degree of methylation of long interspersed nucleotide elements (L1s), in peripheral blood mononuclear cell (PBMC) DNA, a documented biomarker of CIN risk.]. 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:25302494 ;
    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:NP1228085.RAmMfbzzz4JVX86MJ8U8S3zef-yJo3wcE0tihNH4lM8b8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:02+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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> ;
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}