@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk> .
@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:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_head {
  this: np:hasAssertion dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_assertion;
    np:hasProvenance dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_provenance;
    np:hasPublicationInfo dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_assertion a np:Assertion .
  
  dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_provenance a np:Provenance .
  
  dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_assertion {
  miriam-gene:2004 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGNf79946f8fdc74295aa7f532e43600794 sio:SIO_000628 miriam-gene:2004, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_provenance {
  dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_assertion dcterms:description
      "[As the individual P3 latency of the majority of HD patients and all presymptomatic gene carriers was distributed within normal confidence intervals, and no correlation existed between ERP parameters and the signs of illness progression, the data appear to provide preliminary evidence against the valence of P3 in detecting the early cognitive impairment of HD.]. 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:15008503;
    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:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:13+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" .
}