@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio> .
@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:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_head {
  this: np:hasAssertion dgn-np:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_assertion;
    np:hasProvenance dgn-np:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_provenance;
    np:hasPublicationInfo dgn-np:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_assertion a np:Assertion .
  
  dgn-np:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_provenance a np:Provenance .
  
  dgn-np:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_assertion {
  miriam-gene:5629 a ncit:C16612 .
  
  lld:C0024291 a ncit:C7057 .
  
  dgn-gda:DGN3962cbe7d740f82c8999601b91b0f569 sio:SIO_000628 miriam-gene:5629, lld:C0024291;
    a sio:SIO_001121 .
}

dgn-np:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_provenance {
  dgn-np:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_assertion dcterms:description
      "[We suggest that dysregulation of PROX1 gene expression due to separation from its conserved upstream elements is likely to have caused the heart defects observed in this patient, and that PROX1 should be considered as a potential candidate gene for other cases of HLH.]. 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:19471316;
    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:NP326034.RA4V23MRz4RfVLQbOyd2vvHZVm5zj9UE3tMfxSDm47cio130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:10+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" .
}