@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM> .
@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:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_head {
   this: np:hasAssertion dgn-np:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_assertion ;
    np:hasProvenance dgn-np:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_provenance ;
    np:hasPublicationInfo dgn-np:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_assertion a np:Assertion .
  dgn-np:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_provenance a np:Provenance .
  dgn-np:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_assertion {
   miriam-gene:124590 a ncit:C16612 .
  lld:C0871099 a ncit:C7057 .
  dgn-gda:DGNe86fe90589e0590a7338ffc20f3317e0 sio:SIO_000628 miriam-gene:124590 , lld:C0871099 ;
    a sio:SIO_001121 .
}
dgn-np:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_provenance {
   dgn-np:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_assertion dcterms:description "[The ascertainment protocol for data collection included blood sample, structured Diagnostic Interview for Genetic Studies (DIGS), Structured Interview for Schizotypy (SIS), scales for assessment of positive and negative symptoms (SAPS, SANS), and continuous performance test (CPT), Wisconsin card sort test (WCST) of neuropsychological functions.]. 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:15685625 ;
    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:NP899764.RA3YVejrt7CQKNV2wkWr5dORWPl1OgWwK2Faoz4tfXrgM130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:13+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" .
}