@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8> .
@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:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_head {
  this: np:hasAssertion dgn-np:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_assertion;
    np:hasProvenance dgn-np:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_provenance;
    np:hasPublicationInfo dgn-np:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_assertion a np:Assertion .
  
  dgn-np:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_provenance a np:Provenance .
  
  dgn-np:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_assertion {
  miriam-gene:2066 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGNdb381e3351bc2c8c9b2f116d9bff4f46 sio:SIO_000628 miriam-gene:2066, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_provenance {
  dgn-np:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_assertion dcterms:description
      "[We hypothesised that variation in the gene encoding the NRG1 receptor, ErbB4, would also be associated with reduced ALIC integrity and with cognitive impairments characteristic of individuals with bipolar disorder and 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:21232925;
    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:NP381131.RA4fgXRduEL6_0wW2ClteE09tBeOGojL1CFcJKLR48Us8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:20+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" .
}