@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg> .
@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:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_head {
  this: np:hasAssertion dgn-np:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_assertion;
    np:hasProvenance dgn-np:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_provenance;
    np:hasPublicationInfo dgn-np:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_assertion a np:Assertion .
  
  dgn-np:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_provenance a np:Provenance .
  
  dgn-np:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_assertion {
  miriam-gene:2354 a ncit:C16612 .
  
  lld:C0023524 a ncit:C7057 .
  
  dgn-gda:DGN19b247cc6afb2136dc01d0f2a601aa2b sio:SIO_000628 miriam-gene:2354, lld:C0023524;
    a sio:SIO_001121 .
}

dgn-np:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_provenance {
  dgn-np:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_assertion dcterms:description
      "[In eight of these (80%) additional juxtapositioned nuclear factor 1, glial factor 1 and/or AP-1 binding motifs were created by duplications and/or insertions in region D. These findings indicate that type II TCRs are frequently present in PML and suggest to use TCR type II constructs for in vitro and in vivo studies of the evaluation of the functional role of DNA binding motifs.]. 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:11031693;
    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:NP862333.RAnZdcXuz6P62K32aL4EpRx4o3K4W8LX3rdkoJ8nyCQqg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:47+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" .
}