@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_head {
  this: np:hasAssertion dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_assertion;
    np:hasProvenance dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_provenance;
    np:hasPublicationInfo dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_assertion a np:Assertion .
  
  dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_provenance a np:Provenance .
  
  dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_assertion {
  miriam-gene:1296 a ncit:C16612 .
  
  lld:C0010036 a ncit:C7057 .
  
  dgn-gda:DGNda5aa08053f3bd91a328b32bb0c1b991 sio:SIO_000628 miriam-gene:1296, lld:C0010036;
    a sio:SIO_001121 .
}

dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_provenance {
  dgn-np:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_assertion dcterms:description
      "[The absence of pathogenic mutations identified in the COL8A1 or COL8A2 genes in affected members of 15 pedigrees with familial FECD indicates that other genetic factors are involved in the development of this autosomal dominant corneal dystrophy.]. 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:16936088;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP566229.RAH7BaT6TXMBSJdC1SEYTL7KrolIhtOFkXJRnlEvP_woY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:01+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}