@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_head {
   this: np:hasAssertion dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_assertion ;
    np:hasProvenance dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_provenance ;
    np:hasPublicationInfo dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_assertion a np:Assertion .
  dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_provenance a np:Provenance .
  dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_assertion {
   miriam-gene:93986 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGNf59168d441ea2fab296e939e92b5aba7 sio:SIO_000628 miriam-gene:93986 , lld:C0036341 ;
    a sio:SIO_001121 .
}
dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_provenance {
   dgn-np:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_assertion dcterms:description "[We screened the coding trinucleotide repeats of OTX1, EN1, DLX2, HOXA1, and FOXP2 genes in populations suffering from schizophrenia (247 patients), autism (98 patients), and idiopathic mental retardation (56 patients), and compared them with control populations (112 super controls and 202 healthy controls).]. 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:19018235 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP962548.RAAr8A45WNBlzoaOcxflbH1GQmrKnoyJ4x4SB9uhbgkRg130_publicationInfo {
   this: dcterms:created "2015-08-25T14:47:28+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}