@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk> .
@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:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_head {
  this: np:hasAssertion dgn-np:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_assertion;
    np:hasProvenance dgn-np:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_provenance;
    np:hasPublicationInfo dgn-np:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_assertion a np:Assertion .
  
  dgn-np:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_provenance a np:Provenance .
  
  dgn-np:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_assertion {
  miriam-gene:1296 a ncit:C16612 .
  
  lld:C0010036 a ncit:C7057 .
  
  dgn-gda:DGN4296de585bbf68d4e404c4789efa79ca sio:SIO_000628 miriam-gene:1296, lld:C0010036;
    a sio:SIO_001121 .
}

dgn-np:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_provenance {
  dgn-np:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_assertion dcterms:description
      "[To determine whether Japanese patients with Fuchs' endothelial corneal dystrophy (FECD) and posterior polymorphous dystrophy (PPMD) carry mutations in the COL8A2 gene, and to investigate the possible pathogenicity of the COL8A2 gene in these corneal dystrophies.]. 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:15175909;
    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:NP539699.RAlyiqrK8rEY81qLVl7qyoyoyetr7IID9w7ep4kigfzQk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:25+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" .
}