@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ> .
@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:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_head {
  this: np:hasAssertion dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_assertion;
    np:hasProvenance dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_provenance;
    np:hasPublicationInfo dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_assertion a np:Assertion .
  
  dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_provenance a np:Provenance .
  
  dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_assertion {
  miriam-gene:907 a ncit:C16612 .
  
  lld:C0339573 a ncit:C7057 .
  
  dgn-gda:DGNa56eddc79c0fffb332e0ca4c6fdf4dd7 sio:SIO_000628 miriam-gene:907, lld:C0339573;
    a sio:SIO_001121 .
}

dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_provenance {
  dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_assertion dcterms:description
      "[One approach to identify genes that contribute to common complex ocular disorders such as primary open angle glaucoma (POAG) is to study the genetic determinates of endophenotypes that are defined by underlying pre-disposing heritable quantitative traits such as central corneal thickness (CCT).]. 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:21139683;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:50+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" .
}