@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck> .
@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:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_head {
  this: np:hasAssertion dgn-np:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_assertion;
    np:hasProvenance dgn-np:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_provenance;
    np:hasPublicationInfo dgn-np:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_assertion a np:Assertion .
  
  dgn-np:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_provenance a np:Provenance .
  
  dgn-np:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_assertion {
  miriam-gene:3064 a ncit:C16612 .
  
  lld:C0393584 a ncit:C7057 .
  
  dgn-gda:DGNd950fab8ec6ff33ffb8c473b9e3ef1ef sio:SIO_000628 miriam-gene:3064, lld:C0393584;
    a sio:SIO_001121 .
}

dgn-np:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_provenance {
  dgn-np:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_assertion dcterms:description
      "[Using primers flanking the (CAG)n repeat in IT15, expansion of which is associated with HD, we have detected an abnormal PCR product in four affected members from one family where affected subjects were originally reported to have BHC.]. 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:8133497;
    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:NP854517.RAJFxM3O0XFHmXXOQB0M9UhHAEW8sClMr3GE7WrLPg2ck130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:42+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" .
}