@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78> .
@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:NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78130_head {
  this: np:hasAssertion dgn-np:NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78130_assertion ;
    np:hasProvenance dgn-np:NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78130_provenance ;
    np:hasPublicationInfo dgn-np:NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78130_provenance a np:Provenance .
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}
dgn-np:NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78130_assertion {
  miriam-gene:1815 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGN037cef1dd7a9b38b72f5c446377955b2 sio:SIO_000628 miriam-gene:1815 , lld:C0036341 ;
    a sio:SIO_001121 .
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dgn-np:NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78130_provenance {
  dgn-np:NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78130_assertion dcterms:description "[We firstly examined the SNPs in functional genomic regions, such as mRNA splicing, protein coding and the promoter regions in DRD2, DRD3 and DRD4, respectively, for association in 289 Han Chinese cases with schizophrenia and 367 healthy controls and then further analyzed the significantly associated single nucleotide polymorphisms (SNPs) with this disorder in an additional Han Chinese sample consisted of 1351 cases and 1640 control subjects.]. 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:22569179 ;
    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:NP232419.RAp0wiFx4hWG2-S3nL6fwBmKQin9STWLTGy1ekMBRFw78130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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