@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M> .
@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:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_head {
  this: np:hasAssertion dgn-np:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_assertion;
    np:hasProvenance dgn-np:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_provenance;
    np:hasPublicationInfo dgn-np:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_assertion a np:Assertion .
  
  dgn-np:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_provenance a np:Provenance .
  
  dgn-np:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_assertion {
  miriam-gene:26047 a ncit:C16612 .
  
  lld:C0018817 a ncit:C7057 .
  
  dgn-gda:DGNd8d540aaafb4723640fd3864286e760f sio:SIO_000628 miriam-gene:26047, lld:C0018817;
    a sio:SIO_001121 .
}

dgn-np:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_provenance {
  dgn-np:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_assertion dcterms:description
      "[Nonetheless, when viewed in light of two independent studies published in this issue of AJHG showing a relationship between ASD and common CNTNAP2 alleles, the cytogenetic and mutation screening data suggest that rare variants may also contribute to the pathophysiology of ASD, but place limits on the magnitude of this contribution.]. 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:18179895;
    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:NP648734.RAkGy3DReFkaGwColN61MlV1tYc7xTeiLxCJahQsNld9M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:39+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" .
}