@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ> .
@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:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_head {
  this: np:hasAssertion dgn-np:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_assertion;
    np:hasProvenance dgn-np:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_provenance;
    np:hasPublicationInfo dgn-np:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_assertion a np:Assertion .
  
  dgn-np:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_provenance a np:Provenance .
  
  dgn-np:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_assertion {
  miriam-gene:2690 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGN195ba9a11955d5ece5b5623d4d40a82a sio:SIO_000628 miriam-gene:2690, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_provenance {
  dgn-np:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_assertion dcterms:description
      "[Our findings suggest that the level of genetic loading may have a dose-dependent effect on cortical thinning in the right ACC and in the left paracingulate cortex and that cortical thinning in GHR subjects may represent neurodevelopmental alterations that result from genetic liability for schizophrenia.]. 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:22998933;
    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:NP671916.RAhxYjT9kzKn-XlRZVbcBvU6DHvbfGsW--0AqxyN594IQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:45+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" .
}