@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ> .
@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:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_head {
  this: np:hasAssertion dgn-np:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_assertion;
    np:hasProvenance dgn-np:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_provenance;
    np:hasPublicationInfo dgn-np:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_assertion a np:Assertion .
  
  dgn-np:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_provenance a np:Provenance .
  
  dgn-np:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_assertion {
  miriam-gene:7166 a ncit:C16612 .
  
  lld:C0023890 a ncit:C7057 .
  
  dgn-gda:DGN4e089807ab26c3b922d4b183a0e58b78 sio:SIO_000628 miriam-gene:7166, lld:C0023890;
    a sio:SIO_001122 .
}

dgn-np:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_provenance {
  dgn-np:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_assertion dcterms:description
      "[Polymorphisms in genes involved in the regulation of angiogenesis are associated with the risk of HPS. Further investigation of these biologic pathways might elucidate the mechanisms that mediate the development of HPS in certain patients with severe live]. 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:20346360;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP148226.RAdrk874BBfKid093F9phECF-HRIDCSRXRefXfw58HhGQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:03+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" .
}