@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA> .
@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:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_head {
  this: np:hasAssertion dgn-np:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_assertion;
    np:hasProvenance dgn-np:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_provenance;
    np:hasPublicationInfo dgn-np:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_assertion a np:Assertion .
  
  dgn-np:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_provenance a np:Provenance .
  
  dgn-np:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_assertion {
  miriam-gene:80331 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGNb68d9f48de3e2a2ac0fe3731ea4bab7a sio:SIO_000628 miriam-gene:80331, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_provenance {
  dgn-np:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_assertion dcterms:description
      "[Most childhood forms of NCL are clinically characterized by progressive loss of vision as well as mental and motor deterioration, epileptic seizures, and premature death, while the rare adult forms are dominated by dementia.]. 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:16908122;
    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:NP289259.RAVuEFG87x-2JJi6zBEF7R77wAov90TuP37Id7JCnq6hA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:44+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" .
}