@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ> .
@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:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_head {
  this: np:hasAssertion dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_assertion ;
    np:hasProvenance dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_assertion a np:Assertion .
  dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_provenance a np:Provenance .
  dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0079745 a ncit:C7057 .
  dgn-gda:DGN49b19b40b46e147736c8b8abb866e458 sio:SIO_000628 miriam-gene:4524 , lld:C0079745 ;
    a sio:SIO_001122 .
}
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_provenance {
  dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_assertion dcterms:description "[The aim of our study was to investigate the potential influence of the C677T and A1298C genetic variants of the methylenetetrahydrofolate reductase (MTHFR) gene on the clinical toxicity and efficacy of MTX in pediatric patients with NHL (n = 95) treated with therapeutic protocols Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) LNH-97 and EURO LB-02.]. 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:23488607 ;
    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:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:47+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> ;
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}