@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA> .
@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:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_head {
  this: np:hasAssertion dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_assertion;
    np:hasProvenance dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_provenance;
    np:hasPublicationInfo dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_assertion a np:Assertion .
  
  dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_provenance a np:Provenance .
  
  dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_assertion {
  miriam-gene:9590 a ncit:C16612 .
  
  lld:C0035335 a ncit:C7057 .
  
  dgn-gda:DGN4731bef66453d86075f12eca38f93072 sio:SIO_000628 miriam-gene:9590, lld:C0035335;
    a sio:SIO_001121 .
}

dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_provenance {
  dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_assertion dcterms:description
      "[AKAP12 may induce BRB formation through antiangiogenesis and barriergenesis in developing human eye and defects in this mechanism can lead to loss of tight junction proteins and contribute to development of retinal pathologies such as retinoblastoma.]. 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:17442832;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:56+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" .
}