@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8> .
@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:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_head {
  this: np:hasAssertion dgn-np:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_assertion;
    np:hasProvenance dgn-np:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_provenance;
    np:hasPublicationInfo dgn-np:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_assertion a np:Assertion .
  
  dgn-np:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_provenance a np:Provenance .
  
  dgn-np:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_assertion {
  miriam-gene:7040 a ncit:C16612 .
  
  lld:C0035344 a ncit:C7057 .
  
  dgn-gda:DGN08fb91472e5f302828f5a05fd7b23585 sio:SIO_000628 miriam-gene:7040, lld:C0035344;
    a sio:SIO_001122 .
}

dgn-np:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_provenance {
  dgn-np:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_assertion dcterms:description
      "[ The progression of ROP to threshold ROP in very preterm infants may be influenced by genetic differences in VEGF production. Future efforts at prevention of threshold ROP may be directed toward blocking excess production of VEGF.]. 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:15161830;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP50646.RABIkmOQREw2XhfEjhfAvbE3zTzi_EDHBnMqUbURBuvt8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}