@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_head {
  this: np:hasAssertion dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_assertion;
    np:hasProvenance dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_provenance;
    np:hasPublicationInfo dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_assertion a np:Assertion .
  
  dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_provenance a np:Provenance .
  
  dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_assertion {
  miriam-gene:860 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN1d9ad98ebe31957da0359be97bf6bf04 sio:SIO_000628 miriam-gene:860, lld:C0006826;
    a sio:SIO_001122 .
}

dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_provenance {
  dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_assertion dcterms:description
      "[A Runx2 binding site was reported to be functional only in the minor, disease associated allele of rs2981578, resulting in increased expression of FGFR2 in cancers from patients homozygous for that allele.]. 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:24265722;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:22+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}