@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw> .
@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:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_head {
  this: np:hasAssertion dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_assertion;
    np:hasProvenance dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_provenance;
    np:hasPublicationInfo dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_assertion a np:Assertion .
  
  dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_provenance a np:Provenance .
  
  dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_assertion {
  miriam-gene:3702 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN845b4f23461f9224e2faca491e9b1322 sio:SIO_000628 miriam-gene:3702, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_provenance {
  dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_assertion dcterms:description
      "[Taken together, our results demonstrate the roles of multiple microRNAs and p38 signaling in the progression of cancer and demonstrate the therapeutic potential of targeting the p38 MAPK pathway for reversing EMT in an advanced tumor phenotype.]. 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:23403951;
    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:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:53+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" .
}