@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w> .
@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:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_head {
  this: np:hasAssertion dgn-np:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_assertion;
    np:hasProvenance dgn-np:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_provenance;
    np:hasPublicationInfo dgn-np:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_assertion a np:Assertion .
  
  dgn-np:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_provenance a np:Provenance .
  
  dgn-np:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_assertion {
  miriam-gene:9968 a ncit:C16612 .
  
  lld:C0206630 a ncit:C7057 .
  
  dgn-gda:DGNab23bb40acf252a37d2a3a97ae75383c sio:SIO_000628 miriam-gene:9968, lld:C0206630;
    a sio:SIO_001121 .
}

dgn-np:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_provenance {
  dgn-np:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_assertion dcterms:description
      "[Emerging genetic information has also greatly expanded our understanding of 'sarcomagenesis' in both tumour types and may provide insight into potential therapeutic targets for the treatment of leiomyosarcoma and endometrial stromal sarcomas, harboring MED12 (mediator complex subunit 12) mutations and recurrent gene rearrangements, respectively.]. 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:23240674;
    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:NP456151.RAb5SjBx8q9mwi8Tc12yz17HCpLbfagofUU4USwlhLQ8w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:32+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" .
}