@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o> .
@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:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_head {
  this: np:hasAssertion dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_assertion ;
    np:hasProvenance dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_provenance ;
    np:hasPublicationInfo dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_assertion a np:Assertion .
  dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_provenance a np:Provenance .
  dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_assertion {
  miriam-gene:4709 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN586cd2e4f9f4e710d6adde2a292782bc sio:SIO_000628 miriam-gene:4709 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_provenance {
  dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_assertion dcterms:description "[(1990) Cancer Res., 50, 5049-5054], the seven individuals with the highest observed frequencies of micronucleated erythrocytes all had exceptionally low values of plasma folate, red cell folate, or plasma B12, suggesting that folate and B12 status are the major determinants of the types of damage that lead to spontaneous micronucleus formation in erythrocytic cells.]. 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:9219587 ;
    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:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}