@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc> .
@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/v4.0.0/void/> .

dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_head {
  this: np:hasAssertion dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_assertion;
    np:hasProvenance dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_provenance;
    np:hasPublicationInfo dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_assertion a np:Assertion .
  
  dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_provenance a np:Provenance .
  
  dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_assertion {
  miriam-gene:414 a ncit:C16612 .
  
  lld:C1510586 a ncit:C7057 .
  
  dgn-gda:DGN2d2a56721506b5644622653701bdf170 sio:SIO_000628 miriam-gene:414, lld:C1510586;
    a sio:SIO_001121 .
}

dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_provenance {
  dgn-np:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_assertion dcterms:description
      "[Here we present the results from a whole-genome CNV study on a cohort of 859 ASD cases and 1,409 healthy children of European ancestry who were genotyped with approximately 550,000 single nucleotide polymorphism markers, in an attempt to comprehensively identify CNVs conferring susceptibility to ASDs.]. 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:19404257;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP735572.RAYrOVpj84gn_8lR0dqShluidyEFfDua6sF2hHuoBHDnc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:18+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}