@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08> .
@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:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_head {
  this: np:hasAssertion dgn-np:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_assertion;
    np:hasProvenance dgn-np:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_provenance;
    np:hasPublicationInfo dgn-np:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_assertion a np:Assertion .
  
  dgn-np:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_provenance a np:Provenance .
  
  dgn-np:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_assertion {
  miriam-gene:1349 a ncit:C16612 .
  
  lld:C0796070 a ncit:C7057 .
  
  dgn-gda:DGN19a1d2933d8b3b6a8ac40796c5793584 sio:SIO_000628 miriam-gene:1349, lld:C0796070;
    a sio:SIO_001121 .
}

dgn-np:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_provenance {
  dgn-np:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_assertion dcterms:description
      "[Downregulation of the COX7B ortholog (cox7B) in medaka (Oryzias latipes) resulted in microcephaly and microphthalmia that recapitulated the MLS phenotype and demonstrated an essential function of complex IV activity in vertebrate CNS development.]. 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:23122588;
    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:NP398293.RAnwgXQcLNWb821Qkp6Ia-zfgzYe69HhgXjwN4sa8D_08130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:57+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" .
}