@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_head {
  this: np:hasAssertion dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_assertion;
    np:hasProvenance dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_provenance;
    np:hasPublicationInfo dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_assertion a np:Assertion .
  
  dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_provenance a np:Provenance .
  
  dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_assertion {
  miriam-gene:85300 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGN14cd247dcee277eb0c142a6d605e8110 sio:SIO_000628 miriam-gene:85300, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_provenance {
  dgn-np:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_assertion dcterms:description
      "[Mutations in Atcay/ATCAY have been identified as causative of cerebellar disorders such as the rare hereditary disease Cayman ataxia in humans, generalized dystonia in the dystonic (dt) rat, and marked motor defects in three ataxic mouse lines.]. 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:23226316;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP958851.RAN3-nsIQt-R3sa8eJtuds4B77cYkhGR0jHWirmqQi4Fc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:25+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}