@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y> .
@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:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_head {
  this: np:hasAssertion dgn-np:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_assertion;
    np:hasProvenance dgn-np:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_provenance;
    np:hasPublicationInfo dgn-np:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_assertion a np:Assertion .
  
  dgn-np:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_provenance a np:Provenance .
  
  dgn-np:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_assertion {
  miriam-gene:2066 a ncit:C16612 .
  
  lld:C0349204 a ncit:C7057 .
  
  dgn-gda:DGN71f77b0a9c68029d7511916496b8aa2c sio:SIO_000628 miriam-gene:2066, lld:C0349204;
    a sio:SIO_001121 .
}

dgn-np:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_provenance {
  dgn-np:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_assertion dcterms:description
      "[We performed Sanger sequencing of all 28 exons in ERBB4, as well as part of the promoter and part of the 3'UTR sequence, hypothesizing that rare deleterious variants would be found in 188 cases with mood-incongruent psychosis from the GAIN BP study.]. 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:21637803;
    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:NP509736.RATLcr1asRmF2HpJRURAOT5oaZqU6SQ42KVUpAbGagE0Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:04+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" .
}