@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI> .
@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:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_head {
  this: np:hasAssertion dgn-np:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_assertion;
    np:hasProvenance dgn-np:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_provenance;
    np:hasPublicationInfo dgn-np:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_assertion a np:Assertion .
  
  dgn-np:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_provenance a np:Provenance .
  
  dgn-np:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_assertion {
  miriam-gene:4548 a ncit:C16612 .
  
  lld:C0024299 a ncit:C7057 .
  
  dgn-gda:DGN9e5560a4f78e08131c2596b15d6ff32f sio:SIO_000628 miriam-gene:4548, lld:C0024299;
    a sio:SIO_001122 .
}

dgn-np:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_provenance {
  dgn-np:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_assertion dcterms:description
      "[We have previously reported associations between lymphoma risk and germline polymorphisms in genes of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) and methionine synthase (MTR A2756G), finding the genotype other than the MTHFR 677CC/1298AA to confer a half-risk compared to the MTHFR 677CC/1298AA and a 3-fold higher risk with the MTR GG genotype than the AA/AG genotypes.]. 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:15551285;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP61579.RAfei5o_QikeF2xQl5lV19UkVE-IdkU4Uh7XRBIZS4VVI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}