@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So> .
@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:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_head {
  this: np:hasAssertion dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_assertion;
    np:hasProvenance dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_provenance;
    np:hasPublicationInfo dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_assertion a np:Assertion .
  
  dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_provenance a np:Provenance .
  
  dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0023449 a ncit:C7057 .
  
  dgn-gda:DGN661959b82a4383a405d6b122d0fe63fb sio:SIO_000628 miriam-gene:4524, lld:C0023449;
    a sio:SIO_001121 .
}

dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_provenance {
  dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_assertion dcterms:description
      "[No significant associations between specific MTHFR variants or combinations of variants and risk of ALL were observed neither in the total patient group nor in analyses stratified by gender, age at diagnosis, DNA index, immunophenotype, or TEL/AML1 rearrangement.]. 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:15921520;
    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:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:30+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>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}