@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI> .
@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:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_head {
  this: np:hasAssertion dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_assertion ;
    np:hasProvenance dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_provenance ;
    np:hasPublicationInfo dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_assertion a np:Assertion .
  dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_provenance a np:Provenance .
  dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_assertion {
  miriam-gene:1814 a ncit:C16612 .
  lld:C0011581 a ncit:C7057 .
  dgn-gda:DGN476aa4998c95e418d414b88d721b7b74 sio:SIO_000628 miriam-gene:1814 , lld:C0011581 ;
    a sio:SIO_001121 .
}
dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_provenance {
  dgn-np:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_assertion dcterms:description "[In a sample of 308 Chinese Han patients with major depressive disorder, 13 single nucleotide polymorphisms (SNPs) in coding regions of six genes (MAOA, SLC6A2, TH, COMT, DRD2, DRD3) with minor allele frequencies >5% were successfully genotyped from an initial series of 35 SNPs in 11 candidate genes associated with catecholamine neurotransmission.]. 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:21680027 ;
    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:NP501860.RAekOsv_cQdBXj9IjyZ2Oj9muVqVqOEWZEaSijzy0CGXI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:59+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" .
}