@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo> .
@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:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_head {
  this: np:hasAssertion dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_assertion;
    np:hasProvenance dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_provenance;
    np:hasPublicationInfo dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_assertion a np:Assertion .
  
  dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_provenance a np:Provenance .
  
  dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_assertion {
  miriam-gene:2274 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGNd51db879fbc6b182364bcee5290e3df0 sio:SIO_000628 miriam-gene:2274, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_provenance {
  dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_assertion dcterms:description
      "[Since transcription factors control all fundamental developmental and homeostatic processes, transcriptional cofactors like FHL2 are likely to contribute to human carcinogenesis and are of clinical importance in various forms of cancer.]. 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:17352216;
    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:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:31+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" .
}