@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI> .
@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:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_head {
  this: np:hasAssertion dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_assertion;
    np:hasProvenance dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_provenance;
    np:hasPublicationInfo dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_assertion a np:Assertion .
  
  dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_provenance a np:Provenance .
  
  dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_assertion {
  miriam-gene:27086 a ncit:C16612 .
  
  lld:C0024299 a ncit:C7057 .
  
  dgn-gda:DGNe5c3a1ec753c6bbd215fdafe2573c6a3 sio:SIO_000628 miriam-gene:27086, lld:C0024299;
    a sio:SIO_001121 .
}

dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_provenance {
  dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_assertion dcterms:description
      "[Our findings suggest that (1) FOXP1 translocation may disrupt the full-length FOXP1 transcript and lead to expression of FOXP1 transcript variants with alternate 5' ends and (2) mechanisms other than translocation and copy number changes are also responsible for FOXP1 overexpression in lymphoma.]. 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:18487996;
    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:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:31+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" .
}