@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA> .
@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:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_head {
  this: np:hasAssertion dgn-np:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_assertion;
    np:hasProvenance dgn-np:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_provenance;
    np:hasPublicationInfo dgn-np:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_assertion a np:Assertion .
  
  dgn-np:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_provenance a np:Provenance .
  
  dgn-np:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0007102 a ncit:C7057 .
  
  dgn-gda:DGN0236ccbe46da7520d844c6467e521f69 sio:SIO_000628 miriam-gene:4524, lld:C0007102;
    a sio:SIO_001121 .
}

dgn-np:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_provenance {
  dgn-np:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_assertion dcterms:description
      "[The present study did not find a reduced risk of colorectal or rectal cancer among those with a variant genotype of the MTHFR polymorphism, but observed rather an increased risk of colon cancer, suggesting that the effects of the MTHFR genotype may differ in populations with different levels of folate intake.]. 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:15533596;
    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:NP186199.RAI3v0vuyANYmoPSgNCuYgXk4YBC9e1v829zaGei8WfdA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:42+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" .
}