{ "items" : [
    { "id" : "http://dbpedia.org/resource/Microcephalin"
      "properties" : {
        "http://www.w3.org/2000/01/rdf-schema#comment" : [ "Microcephalin (MCPH1) is a gene that is expressed during fetal brain development. Certain mutations in MCPH1, when homozygous, cause primary microcephaly — a severely diminished brain. Hence it has been assumed that variants have a role in brain development, but in normal individuals no effect on mental ability or behavior has yet been demonstrated in either this or another similarly studied microcephaly gene, ASPM." ] ,
        "http://xmlns.com/foaf/0.1/name" : [ "microcephaly,",
          "primary autosomal recessive 1" ] ,
        "http://xmlns.com/foaf/0.1/depiction" : [ "http://commons.wikimedia.org/wiki/Special:FilePath/Microcephalin.png" ] ,
        "http://dbpedia.org/ontology/arm" : [ "p" ] ,
        "http://dbpedia.org/ontology/band" : [ "23" ] ,
        "http://dbpedia.org/ontology/chromosome" : [ "8" ] ,
        "http://dbpedia.org/ontology/entrezgene" : [ "79648" ] ,
        "http://dbpedia.org/ontology/hgncid" : [ "6954" ] ,
        "http://dbpedia.org/ontology/omim" : [ 607117 ] ,
        "http://dbpedia.org/ontology/symbol" : [ "MCPH1",
          "Microcephalin, BRIT1",
          "Microcephalin" ] ,
        "http://dbpedia.org/ontology/thumbnail" : [ "http://commons.wikimedia.org/wiki/Special:FilePath/Microcephalin.png?width=300" ] ,
        "http://dbpedia.org/ontology/uniprot" : [ "Q8NEM0"] } } }
