@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc> .
@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:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_head {
  this: np:hasAssertion dgn-np:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_assertion;
    np:hasProvenance dgn-np:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_provenance;
    np:hasPublicationInfo dgn-np:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_assertion a np:Assertion .
  
  dgn-np:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_provenance a np:Provenance .
  
  dgn-np:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_assertion {
  miriam-gene:2896 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGN502b9a2420d5527ed250828dc2ea1746 sio:SIO_000628 miriam-gene:2896, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_provenance {
  dgn-np:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_assertion dcterms:description
      "[Gene expression profiling (GEP) will help to improve the management of MM not only by identifying prognostic subgroups but also by defining molecular pathways that are associated with these subgroups and that are possible targets for future therapies.]. 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:15561686;
    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:NP302115.RAOlQUrzu4M4EWbUr-PTDtXnRHrZGVBTMA0NNL0PDzCTc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:53+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" .
}