@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg> .
@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:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_head {
  this: np:hasAssertion dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_assertion;
    np:hasProvenance dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_provenance;
    np:hasPublicationInfo dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_assertion a np:Assertion .
  
  dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_provenance a np:Provenance .
  
  dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_assertion {
  miriam-gene:11331 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGNd413d79316361ee07c048f9bae9d901d sio:SIO_000628 miriam-gene:11331, lld:C0004352;
    a sio:SIO_001121 .
}

dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_provenance {
  dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_assertion dcterms:description
      "[Studies of this broad autism phenotype (BAP) may provide a potentially important complementary approach for detecting the genes causing autism and defining associated neural circuitry by identifying more refined phenotypes that can be measured quantitatively in both affected and unaffected individuals and that are tied to functioning in particular regions of the brain.]. 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:19414711;
    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:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:09+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: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" .
}