@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk> .
@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:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_head {
  this: np:hasAssertion dgn-np:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_assertion ;
    np:hasProvenance dgn-np:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_provenance ;
    np:hasPublicationInfo dgn-np:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_assertion a np:Assertion .
  dgn-np:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_provenance a np:Provenance .
  dgn-np:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_assertion {
  miriam-gene:10675 a ncit:C16612 .
  lld:C0338656 a ncit:C7057 .
  dgn-gda:DGN2f3d816a4029b5c3464cdbc5e4e5ae7d sio:SIO_000628 miriam-gene:10675 , lld:C0338656 ;
    a sio:SIO_001121 .
}
dgn-np:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_provenance {
  dgn-np:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_assertion dcterms:description "[To determine (1) whether the battery of neuropsychological tests was sufficiently sensitive to find differences between symptomatic patients with Huntington's disease (HD) and clinically asymptomatic individuals carrying the HD gene (AGC) and individuals without the HD gene (NGC) and (2) whether increasing cognitive impairment is found in AGC as compared with NGC.]. 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:12174172 ;
    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:NP560072.RAQLGNcJaG-DPRHP6Wd9E6L0fZOeYIf8G7KBOQ6L-UFzk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:38+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" .
}