@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I> .
@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:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_head {
  this: np:hasAssertion dgn-np:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_assertion ;
    np:hasProvenance dgn-np:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_provenance ;
    np:hasPublicationInfo dgn-np:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_assertion a np:Assertion .
  dgn-np:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_provenance a np:Provenance .
  dgn-np:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_assertion {
  miriam-gene:2066 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
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    a sio:SIO_001122 .
}
dgn-np:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_provenance {
  dgn-np:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_assertion dcterms:description "[Two hundred and twenty-seven unrelated chronic inpatients with schizophrenia were enrolled in the study, and the genetic variation in the polymorphisms of the ERBB4 gene in the patients was compared with that of the control group, which consisted of 223 subjects free of psychiatric illness.]. 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:20600594 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP44987.RA0GRRSSLoyohATKiTJfAc4x_xy-WsRX6CJKgnHw6UY2I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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:disgenetrdf ;
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}