@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg> .
@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:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_head {
  this: np:hasAssertion dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_assertion ;
    np:hasProvenance dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_provenance ;
    np:hasPublicationInfo dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_assertion a np:Assertion .
  dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_provenance a np:Provenance .
  dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_assertion {
  miriam-gene:1814 a ncit:C16612 .
  lld:C0013384 a ncit:C7057 .
  dgn-gda:DGN7bb1a3fe6a158c206f20fc42dd0699ec sio:SIO_000628 miriam-gene:1814 , lld:C0013384 ;
    a sio:SIO_001121 .
}
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_provenance {
  dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_assertion dcterms:description "[As recent observations indicate the dopamine D(3) receptor (DRD3) to modulate both therapeutic action of levodopa and dyskinesia, we reappraised the impact of the DRD3 Ser9Gly polymorphism on development of motor complications in a large scale association study based on the gene bank of the German Competence Network on Parkinson's disease.]. 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:19353703 ;
    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:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:48+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" .
}