@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc> .
@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 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:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_head {
  this: np:hasAssertion dgn-np:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_assertion;
    np:hasProvenance dgn-np:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_provenance;
    np:hasPublicationInfo dgn-np:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_assertion a np:Assertion .
  
  dgn-np:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_provenance a np:Provenance .
  
  dgn-np:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_assertion {
  miriam-gene:6647 a ncit:C16612 .
  
  lld:C0022578 a ncit:C7057 .
  
  dgn-gda:DGNc64c99e6db1a0d3ac0cfb93dd0e89edb sio:SIO_000628 miriam-gene:6647, lld:C0022578;
    a sio:SIO_001122 .
}

dgn-np:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_provenance {
  dgn-np:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_assertion dc:description
      "[The absence of pathogenic mutations in VSX1, SOD1, COL4A3, and COL4A4 genes in our large number of unrelated keratoconus patients indicates that other genetic factors are involved in the development of this disorder; nevertheless, a significant correlation of a few polymorphisms indicates that there could be a link between specific polymorphisms and KC disease.]. 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:20664914;
    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:NP81305.RAd--_smKAnlMS6v79xYfXi0Gor4KjRP8sHVPPUbKFEQc130_publicationInfo {
  this: dc:created "2014-10-02T12:32:40+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}