@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas> .
@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:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_head {
  this: np:hasAssertion dgn-np:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_assertion;
    np:hasProvenance dgn-np:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_provenance;
    np:hasPublicationInfo dgn-np:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_assertion a np:Assertion .
  
  dgn-np:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_provenance a np:Provenance .
  
  dgn-np:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGNf40da34bd61aa40b3b5aee668cec485f sio:SIO_000628 miriam-gene:1312, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_provenance {
  dgn-np:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_assertion dcterms:description
      "[This interaction between COMT genotype and PD accords well with previous studies that have shown an excess of DA in the PFC in early PD patients and, furthermore, supports the hypothesis that there is an inverted-U shaped functional relationship between PFC DA levels and attentional set formation.]. 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:22351648;
    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:NP260881.RALl82SY1SXGzsPA9EMr27GJ9HcZdAlYzt29e2ZTDVHas130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:25+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" .
}