@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_head {
  this: np:hasAssertion dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_assertion;
    np:hasProvenance dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_provenance;
    np:hasPublicationInfo dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_assertion a np:Assertion .
  
  dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_provenance a np:Provenance .
  
  dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0035528 a ncit:C7057 .
  
  dgn-gda:DGN1163ae152bffff4395e65dad9c85b42a sio:SIO_000628 miriam-gene:4524, lld:C0035528;
    a sio:SIO_001121 .
}

dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_provenance {
  dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_assertion dcterms:description
      "[We tested the hypothesis that methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism, folic acid deficiency and riboflavin deficiency, independently or interactively, are important determinants of genomic stability, cell death, cell proliferation and homocysteine (Hcy) concentration in 9-d human lymphocyte cultures.]. 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:14704292;
    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:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:33+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}