@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY> .
@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:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_head {
  this: np:hasAssertion dgn-np:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_assertion;
    np:hasProvenance dgn-np:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_provenance;
    np:hasPublicationInfo dgn-np:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_assertion a np:Assertion .
  
  dgn-np:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_provenance a np:Provenance .
  
  dgn-np:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_assertion {
  miriam-gene:1545 a ncit:C16612 .
  
  lld:C0017612 a ncit:C7057 .
  
  dgn-gda:DGN46cf3f9a1ee8dfe2bb2ab85030de1349 sio:SIO_000628 miriam-gene:1545, lld:C0017612;
    a sio:SIO_001122 .
}

dgn-np:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_provenance {
  dgn-np:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_assertion dcterms:description
      "[Although no major effect of common variation at the CYP1B1 locus on POAG was found, there could be an effect of SNPs tagged by rs162562 and represented on the AGCAGCC haplotype.]. 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:21139974;
    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:NP76580.RA4OW_WyN4xuyt0Dr4paGl9ZgtY9hrKP0wz2gJgoDHWaY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:37+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" .
}