@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg> .
@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:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_head {
  this: np:hasAssertion dgn-np:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_assertion ;
    np:hasProvenance dgn-np:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_provenance ;
    np:hasPublicationInfo dgn-np:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_assertion a np:Assertion .
  dgn-np:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_provenance a np:Provenance .
  dgn-np:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_assertion {
  miriam-gene:4128 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGN4405c4291935210ce64d4ec2f723925b sio:SIO_000628 miriam-gene:4128 , lld:C0036341 ;
    a sio:SIO_001122 .
}
dgn-np:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_provenance {
  dgn-np:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_assertion dcterms:description "[These data do not suggest that the MAOA gene VNTR and MAOB gene A644G polymorphisms are associated with antipsychotic-induced RLS symptoms in schizophrenia. However, we found that the haplotype frequencies differed between the male schizophrenic patients with and without RLS symptom and the interaction between the two polymorphisms had a significant influence on the RLS scores of patients 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:20589923 ;
    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:NP54993.RA58SzLkEinLWi3CbeFiMgeosuJ7laIGG-Axv5azc9-wg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}