@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90> .
@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:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_head {
  this: np:hasAssertion dgn-np:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_assertion;
    np:hasProvenance dgn-np:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_provenance;
    np:hasPublicationInfo dgn-np:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_assertion a np:Assertion .
  
  dgn-np:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_provenance a np:Provenance .
  
  dgn-np:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  
  lld:C2678061 a ncit:C7057 .
  
  dgn-gda:DGNaa9f9320ca337db147c5d527f6bd6d80 sio:SIO_000628 miriam-gene:1813, lld:C2678061;
    a sio:SIO_001121 .
}

dgn-np:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_provenance {
  dgn-np:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_assertion dcterms:description
      "[We used (11)C-raclopride PET, a marker of D(2) dopamine receptor binding, and statistical parametric mapping (SPM) to localise cortical D(2) receptor dysfunction in individual Huntington's disease (HD) gene carriers (16 symptomatic and 11 premanifest subjects) and assess its clinical significance.]. 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:19853661;
    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:NP523165.RAnK5S4yRyWOwlA5n99AlpXRZNsjTXt_J4rXM03QNAt90130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:11+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" .
}