@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA> .
@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:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_head {
  this: np:hasAssertion dgn-np:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_assertion;
    np:hasProvenance dgn-np:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_provenance;
    np:hasPublicationInfo dgn-np:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_assertion a np:Assertion .
  
  dgn-np:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_provenance a np:Provenance .
  
  dgn-np:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_assertion {
  miriam-gene:2332 a ncit:C16612 .
  
  lld:C0005586 a ncit:C7057 .
  
  dgn-gda:DGN7b74b308691c18c8cc5777f2f5e390ae sio:SIO_000628 miriam-gene:2332, lld:C0005586;
    a sio:SIO_001121 .
}

dgn-np:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_provenance {
  dgn-np:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_assertion dcterms:description
      "[In this review we discuss the mutation in the fragile X mental retardation-1 gene (FMR1), that leads to FXS, the role FMRP plays in neuronal cells, experiments from our own laboratory that demonstrate reductions of FMRP in additional psychiatric disorders (autism, schizophrenia, bipolar disorder, and major depressive disorder), and potential therapies to ameliorate the loss of FMRP.]. 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:21108954;
    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:NP532678.RA6iXLLnvtUN_xCLLFNPV60250-jFiP7ikRaJ0TdEPMAA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+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" .
}