@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA> .
@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:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_head {
  this: np:hasAssertion dgn-np:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_assertion;
    np:hasProvenance dgn-np:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_provenance;
    np:hasPublicationInfo dgn-np:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_assertion a np:Assertion .
  
  dgn-np:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_provenance a np:Provenance .
  
  dgn-np:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_assertion {
  miriam-gene:8621 a ncit:C16612 .
  
  lld:C0016781 a ncit:C7057 .
  
  dgn-gda:DGN633fca3f18c3f2c97f3b75521dff2786 sio:SIO_000628 miriam-gene:8621, lld:C0016781;
    a sio:SIO_001121 .
}

dgn-np:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_provenance {
  dgn-np:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_assertion dcterms:description
      "[This group of conditions includes Fuchs' endothelial dystrophy of the cornea (FECD), one of the commonest indications for corneal transplantation performed in developed countries, posterior polymorphous dystrophy (PPCD) and the congenital hereditary endothelial dystrophies (CHED).]. 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:11689488;
    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:NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:24+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" .
}