@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI> .
@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:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_head {
  this: np:hasAssertion dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_assertion ;
    np:hasProvenance dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_provenance ;
    np:hasPublicationInfo dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_assertion a np:Assertion .
  dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_provenance a np:Provenance .
  dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_provenance {
  dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_assertion dcterms:description "[Our results will assist in the interpretation of the controversy generated by genetic associations of COMT and schizophrenia, which could be the result of different LD patterns between COMT markers and the 3' region of the ARVCF gene.]. 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:19508883 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:22+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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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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  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}