@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc> .
@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:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_head {
  this: np:hasAssertion dgn-np:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_assertion;
    np:hasProvenance dgn-np:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_provenance;
    np:hasPublicationInfo dgn-np:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_assertion a np:Assertion .
  
  dgn-np:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_provenance a np:Provenance .
  
  dgn-np:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_assertion {
  miriam-gene:2565 a ncit:C16612 .
  
  lld:C1510586 a ncit:C7057 .
  
  dgn-gda:DGNbec0ce333a46608740f1cb5978c38d13 sio:SIO_000628 miriam-gene:2565, lld:C1510586;
    a sio:SIO_001121 .
}

dgn-np:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_provenance {
  dgn-np:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_assertion dcterms:description
      "[Among these de novo and rare inherited CNVs, there were also examples of genes (ASTN2, GABRG1, and CNTN5) previously implicated by rare CNVs in other neurodevelopmental conditions including autism spectrum disorder (ASD).]. 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:21832240;
    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:NP732533.RAVaKTJAWQAqCV-8FmzxTdcmkpTcKZY4Eu78us_O7BoNc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:24+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" .
}