@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA> .
@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:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_head {
  this: np:hasAssertion dgn-np:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_assertion;
    np:hasProvenance dgn-np:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_provenance;
    np:hasPublicationInfo dgn-np:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_assertion a np:Assertion .
  
  dgn-np:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_provenance a np:Provenance .
  
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      np:PublicationInfo .
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dgn-np:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0684249 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_provenance {
  dgn-np:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_assertion dcterms:description
      "[Authors report the results of four meta-analyses of studies that examined the association between methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and head and neck cancer (nine studies, 2076 cases and 4834 controls for C677T; four studies, 1439 cases and 3941 controls for A1298C), and lung cancer (ten studies, 5274 cases and 7435 controls for C677T; seven studies, 5098 cases and 6243 controls for A1298C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP331791.RApxbX2jsRaN5cta_FmBT6d1SEF43Fk5pprAkFQsap-bA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:15+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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