@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI> .
@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:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_head {
  this: np:hasAssertion dgn-np:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_assertion;
    np:hasProvenance dgn-np:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_provenance;
    np:hasPublicationInfo dgn-np:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_assertion a np:Assertion .
  
  dgn-np:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_provenance a np:Provenance .
  
  dgn-np:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_assertion {
  miriam-gene:4552 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGN702923af9546b60ead3a976856ad3892 sio:SIO_000628 miriam-gene:4552, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_provenance {
  dgn-np:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_assertion dcterms:description
      "[In this study, the allelic frequencies and genotype distribution of three polymorphisms in the MTHFR and MTRR genes from 96 hepatocellular carcinoma (HCC) patients and 201 controls were examined to assess the association between these polymorphisms and the development of HCC in this Korean population.]. 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:19035314;
    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:NP512057.RAliGgwwCeZ2l7xf3RGNn7othFs2vY2YsenBRhUrbdzzI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:05+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" .
}