@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4> .
@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:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_head {
  this: np:hasAssertion dgn-np:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_assertion;
    np:hasProvenance dgn-np:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_provenance;
    np:hasPublicationInfo dgn-np:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_assertion a np:Assertion .
  
  dgn-np:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_provenance a np:Provenance .
  
  dgn-np:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_assertion {
  miriam-gene:81832 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGNdec6c8445e086239f39a3297b1983dc1 sio:SIO_000628 miriam-gene:81832, lld:C0004352;
    a sio:SIO_001121 .
}

dgn-np:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_provenance {
  dgn-np:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_assertion dcterms:description
      "[We searched for genetic determinants of autism by (1) identifying additional chromosome copy number changes (2) Identifying common regions of hemizygosity on 18q, and (3) evaluating four regions containing candidate genes located on 18q (MBD1, TCF4, NETO1, FBXO15).]. 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:20499253;
    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:NP728044.RAyIHn8XJfesbpBYlZnCyoM-ZDGoKF-Ysn4buQLdU_QS4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:22+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" .
}