@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w> .
@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:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_head {
  this: np:hasAssertion dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_assertion ;
    np:hasProvenance dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_provenance ;
    np:hasPublicationInfo dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_assertion a np:Assertion .
  dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_provenance a np:Provenance .
  dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_assertion {
  miriam-gene:2260 a ncit:C16612 .
  lld:C0042133 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_provenance {
  dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_assertion dcterms:description "[The integrative genomic and transcriptomic approach indicated that FGFR1 and IGFBP5 amplification, as well as the consequent up-regulation of the protein products, plays an important role in the aetiology of ULs and thus provides data for potential drug therapies development to target genes associated with cellular proliferation in ULs.]. 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:23483937 ;
    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 ;
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}
dgn-np:NP685807.RACmfWujdoCUw9CNAJDa9US0LEvVEHmogaZkRIq7VnR9w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:57+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 ;
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}