@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I> .
@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:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_head {
  this: np:hasAssertion dgn-np:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_assertion;
    np:hasProvenance dgn-np:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_provenance;
    np:hasPublicationInfo dgn-np:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_assertion a np:Assertion .
  
  dgn-np:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_provenance a np:Provenance .
  
  dgn-np:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_assertion {
  miriam-gene:1026 a ncit:C16612 .
  
  lld:C1458155 a ncit:C7057 .
  
  dgn-gda:DGN804f8a02b7ea16da7adb3fa44051ec8e sio:SIO_000628 miriam-gene:1026, lld:C1458155;
    a sio:SIO_001123 .
}

dgn-np:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_provenance {
  dgn-np:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_assertion dcterms:description
      "[Data indicate that overexpression of the transcriptional cofactor FHL2 contributes to breast cancer development by mediating transcriptional activation of MAPK target genes known to be involved in cancer progression, such as p21.]. 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:17682292;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP108357.RAUlV3s0_FNpwfnlGg0c51UdrC0w-PA44v68HXcOwuk2I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:55+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" .
}