@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw> .
@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:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_head {
   this: np:hasAssertion dgn-np:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_assertion ;
    np:hasProvenance dgn-np:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_provenance ;
    np:hasPublicationInfo dgn-np:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_assertion a np:Assertion .
  dgn-np:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_provenance a np:Provenance .
  dgn-np:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_assertion {
   miriam-gene:57680 a ncit:C16612 .
  lld:C3714756 a ncit:C7057 .
  dgn-gda:DGNc7ce519400c390ea81f22c656e1cb40e sio:SIO_000628 miriam-gene:57680 , lld:C3714756 ;
    a sio:SIO_001121 .
}
dgn-np:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_provenance {
   dgn-np:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_assertion dcterms:description "[Overall, 16p11.2 CNV was associated with altered expression of genes and networks that converge on multiple hypotheses of ASD pathogenesis, including synaptic function (e.g., NRXN1, NRXN3), chromatin modification (e.g., CHD8, EHMT1, MECP2), transcriptional regulation (e.g., TCF4, SATB2), and intellectual disability (e.g., FMR1, CEP290).]. 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:24906019 ;
    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:NP932875.RAWiTcFHe3r8UtHiAAJU1_McUfH64dkI3WEFVH5EMeGlw130_publicationInfo {
   this: dcterms:created "2015-08-25T14:47:09+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" .
}