@prefix foaf:    <http://xmlns.com/foaf/0.1/> .
@prefix void:    <http://rdfs.org/ns/void#> .
@prefix up:      <http://purl.uniprot.org/core/> .
@prefix dcterms:  <http://purl.org/dc/terms/> .
@prefix rdfs:    <http://www.w3.org/2000/01/rdf-schema#> .
@prefix ncit:    <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix sio:     <http://semanticscience.org/resource/> .
@prefix xsd:     <http://www.w3.org/2001/XMLSchema#> .
@prefix owl:     <http://www.w3.org/2002/07/owl#> .
@prefix rdf:     <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix skos:    <http://www.w3.org/2004/02/skos/core#> .

<http://rdf.disgenet.org/resource/gda/DGN62f27b11f686fcc408502737f5ee7a4b>
      a       sio:SIO_001121 ;
      rdfs:comment "Association between the gene [ncbigene:203068] and the disease [umls:C0025958] integrated into DisGeNET. Gene-disease associations are identified by the DisGeNET ID."@en ;
      rdfs:label "tubulin, beta class I [ncbigene:203068] - Microcephaly [umls:C0025958] Association [disgenet:DGN62f27b11f686fcc408502737f5ee7a4b]"@en ;
      dcterms:date "2012"^^xsd:gYear ;
      dcterms:description "[Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
      dcterms:identifier "disgenet:DGN62f27b11f686fcc408502737f5ee7a4b"^^xsd:string ;
      dcterms:title "tubulin, beta class I [ncbigene:203068] - Microcephaly [umls:C0025958] Association"@en ;
      up:organism <http://purl.uniprot.org/taxonomy/9606> ;
      void:inDataset <http://rdf.disgenet.org/v4.0.0/void/geneDiseaseAssociation> ;
      sio:SIO_000216 <http://rdf.disgenet.org/resource/gda/ncbigene:203068_umls:C0025958_association_DisGeNETScore> ;
      sio:SIO_000253 <http://rdf.disgenet.org/v4.0.0/void/befree-2016> ;
      sio:SIO_000300 "[Biomarker] association type label in the original source"@en ;
      sio:SIO_000628 <http://linkedlifedata.com/resource/umls/id/C0025958> , <http://identifiers.org/ncbigene/203068> ;
      sio:SIO_000772 <http://identifiers.org/pubmed/23246003> .