@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk> .
@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:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_head {
  this: np:hasAssertion dgn-np:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_assertion;
    np:hasProvenance dgn-np:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_provenance;
    np:hasPublicationInfo dgn-np:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_assertion a np:Assertion .
  
  dgn-np:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_provenance a np:Provenance .
  
  dgn-np:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_assertion {
  miriam-gene:1006 a ncit:C16612 .
  
  lld:C0018817 a ncit:C7057 .
  
  dgn-gda:DGNee5b7bbdd8c09a53ad913f178a7f0310 sio:SIO_000628 miriam-gene:1006, lld:C0018817;
    a sio:SIO_001121 .
}

dgn-np:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_provenance {
  dgn-np:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_assertion dcterms:description
      "[Examples of such intergenic CNV regions include 16q21 and 2p16.3 near known ASD risk genes CDH8 and NRXN1 respectively, as well as novel loci contiguous with ZHX2, MOCS1, LRRC4C, SEMA3C, and other genes.]. 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:23879678;
    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:NP300092.RAS3AmBTFrWAx24iVVCqtSNC4sEeeVrDGEVee_PbTYZHk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:32+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" .
}