@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds> .
@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/v4.0.0/void/> .
dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_head {
  this: np:hasAssertion dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_assertion ;
    np:hasProvenance dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_provenance ;
    np:hasPublicationInfo dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_assertion a np:Assertion .
  dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_provenance a np:Provenance .
  dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_assertion {
  miriam-gene:8863 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGNdcc193af3ca9575e14fb0b26afd7747f sio:SIO_000628 miriam-gene:8863 , lld:C0036341 ;
    a sio:SIO_001122 .
}
dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_provenance {
  dgn-np:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_assertion dcterms:description "[Our results suggest that the T3111C (RS1801260) polymorphism of hClock gene is associated with schizophrenia, but it seems that the length polymorphism of 18 exon of hPer3 may not be associated with 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:20364331 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP168989.RAx2fFsQt7uxVijbIQWSe8uOOsYSqwe3iP1gTeCWM7Fds130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:04+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: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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}