@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8> .
@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:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_head {
  this: np:hasAssertion dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_assertion;
    np:hasProvenance dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_provenance;
    np:hasPublicationInfo dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_assertion a np:Assertion .
  
  dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_provenance a np:Provenance .
  
  dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_assertion {
  miriam-gene:1822 a ncit:C16612 .
  
  lld:C0233794 a ncit:C7057 .
  
  dgn-gda:DGN4d8a22167a5716b1ddfd34c0fbad144c sio:SIO_000628 miriam-gene:1822, lld:C0233794;
    a sio:SIO_001121 .
}

dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_provenance {
  dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_assertion dcterms:description
      "[In this study, we have established DRPLA transgenic mouse lines (sublines) harboring a single copy of the full-length mutant human DRPLA gene carrying various lengths of expanded CAG repeats (Q76, Q96, Q113, and Q129), which have clearly shown motor deficits and memory disturbance whose severity increases with the length of expanded CAG repeats and age, and successfully replicated the CAG repeat length- and age-dependent features of DRPLA patients.]. 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:22342974;
    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:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}