@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8> .
@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:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_head {
  this: np:hasAssertion dgn-np:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_assertion;
    np:hasProvenance dgn-np:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_provenance;
    np:hasPublicationInfo dgn-np:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_assertion a np:Assertion .
  
  dgn-np:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_provenance a np:Provenance .
  
  dgn-np:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_assertion {
  miriam-gene:6573 a ncit:C16612 .
  
  lld:C0585442 a ncit:C7057 .
  
  dgn-gda:DGN89be6499e291be831a02af47bfd4dc06 sio:SIO_000628 miriam-gene:6573, lld:C0585442;
    a sio:SIO_001121 .
}

dgn-np:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_provenance {
  dgn-np:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_assertion dcterms:description
      "[Whereas inactivating RFC mutations are a frequent mechanism of MTX resistance in human leukemia cell lines and in patients with osteosarcoma, they are not common and do not appear to play any significant role in intrinsic or acquired resistance to MTX in childhood leukemia.]. 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:14770434;
    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:NP575429.RAazZczKEaVuuTJnbc5vY9hvS6yuRaHebKPXu8jIfwKH8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:47+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" .
}