@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ> .
@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:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_head {
  this: np:hasAssertion dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_assertion;
    np:hasProvenance dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_provenance;
    np:hasPublicationInfo dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_assertion a np:Assertion .
  
  dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_provenance a np:Provenance .
  
  dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_assertion {
  miriam-gene:4580 a ncit:C16612 .
  
  lld:C0023449 a ncit:C7057 .
  
  dgn-gda:DGN292e04bffe8d8f22295fd1f70ce86254 sio:SIO_000628 miriam-gene:4580, lld:C0023449;
    a sio:SIO_001121 .
}

dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_provenance {
  dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_assertion dcterms:description
      "[Furthermore, analysis of FPGS transcripts in blood or bone marrow specimens from patients with acute lymphoblastic leukemia revealed exon 12 skipping, both at diagnosis and at relapse, the latter of which occurs after high-dose MTX-containing chemotherapy.]. 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:19131550;
    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:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+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" .
}