@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA> .
@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:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_head {
  this: np:hasAssertion dgn-np:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_assertion;
    np:hasProvenance dgn-np:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_provenance;
    np:hasPublicationInfo dgn-np:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_assertion a np:Assertion .
  
  dgn-np:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_provenance a np:Provenance .
  
  dgn-np:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_assertion {
  miriam-gene:1649 a ncit:C16612 .
  
  lld:C0206634 a ncit:C7057 .
  
  dgn-gda:DGN65102cbae8a6cec404efe5dabd5aeaa0 sio:SIO_000628 miriam-gene:1649, lld:C0206634;
    a sio:SIO_001121 .
}

dgn-np:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_provenance {
  dgn-np:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_assertion dcterms:description
      "[Restriction fragment analysis showed that the CHOP gene and its flanking sequences were not rearranged in any of these tumor types, indicating that the 12q translocation breakpoints in pleomorphic adenoma and clear-cell sarcoma are different from that in myxoid liposarcoma.]. 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:7687873;
    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:NP304759.RA4xNf2ULa4HONoe9EIwFb6goiMphvPdiXLs7-OMmm7xA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:55+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" .
}