@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M> .
@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:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_head {
  this: np:hasAssertion dgn-np:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_assertion;
    np:hasProvenance dgn-np:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_provenance;
    np:hasPublicationInfo dgn-np:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_assertion a np:Assertion .
  
  dgn-np:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_provenance a np:Provenance .
  
  dgn-np:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_assertion {
  miriam-gene:6573 a ncit:C16612 .
  
  lld:C0027819 a ncit:C7057 .
  
  dgn-gda:DGN0b13ea91da297fa2bda0338e97ad261c sio:SIO_000628 miriam-gene:6573, lld:C0027819;
    a sio:SIO_001121 .
}

dgn-np:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_provenance {
  dgn-np:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_assertion dcterms:description
      "[Our results suggest that individuals carriers of genotype AA for the SLC19A1 gene present risk for the development of neuroblastoma and possibly have difficulty in absorption of folic acid by the cells, and this may adversely affect the metabolism of folate causing genomic instability and promoting the development of cancer.]. 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:24771227;
    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:NP1177160.RAr4hoCtgZR2L5hHVUtdvZD_GsN8Cd2QFay9EsDWiFC0M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:39+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" .
}