@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI> .
@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:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_head {
  this: np:hasAssertion dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_assertion;
    np:hasProvenance dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_provenance;
    np:hasPublicationInfo dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_assertion a np:Assertion .
  
  dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_provenance a np:Provenance .
  
  dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_assertion {
  miriam-gene:472 a ncit:C16612 .
  
  lld:C0019829 a ncit:C7057 .
  
  dgn-gda:DGN0c51e8a9daea67b23ee3dd10f218b397 sio:SIO_000628 miriam-gene:472, lld:C0019829;
    a sio:SIO_001121 .
}

dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_provenance {
  dgn-np:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_assertion dcterms:description
      "[The frequency of ATM variants was analyzed in the total group of 64 cases of HD and compared to allele frequencies in 128 ethnically matched controls from the same geographical region.]. 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:12473594;
    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:NP649853.RA1qbz0O9jOR5AjbykuzI9ISAb4CLpfF7tHZJqRr65EXI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:31+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" .
}