@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A> .
@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:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_head {
  this: np:hasAssertion dgn-np:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_assertion ;
    np:hasProvenance dgn-np:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_provenance ;
    np:hasPublicationInfo dgn-np:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_assertion a np:Assertion .
  dgn-np:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_provenance a np:Provenance .
  dgn-np:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_assertion {
  miriam-gene:1719 a ncit:C16612 .
  lld:C0023449 a ncit:C7057 .
  dgn-gda:DGN33c48b4b7316a077b10ce810e24819ac sio:SIO_000628 miriam-gene:1719 , lld:C0023449 ;
    a sio:SIO_001121 .
}
dgn-np:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_provenance {
  dgn-np:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_assertion dcterms:description "[The relevance of this phenomenon in clinical samples is unknown but is extremely pertinent in childhood acute lymphoblastic leukaemia (ALL) in which children are exposed for prolonged periods to both MTX and thiopurines such that a single amplification event involving both the DHFR and the MSH3 genes may cause chemotherapeutic resistance to both agents.]. 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:17148505 ;
    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:NP886120.RAduXcgAjk37VlTxO76r-KX3jcTGtumhKrabw-jczj93A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:01+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" .
}