@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek> .
@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/v4.0.0/void/> .

dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_head {
  this: np:hasAssertion dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_assertion;
    np:hasProvenance dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_provenance;
    np:hasPublicationInfo dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_assertion a np:Assertion .
  
  dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_provenance a np:Provenance .
  
  dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_assertion {
  miriam-gene:6311 a ncit:C16612 .
  
  lld:C0752121 a ncit:C7057 .
  
  dgn-gda:DGN3c0b25d9588d895aa9930fa0cb34a53b sio:SIO_000628 miriam-gene:6311, lld:C0752121;
    a sio:SIO_001121 .
}

dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_provenance {
  dgn-np:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_assertion dcterms:description
      "[This family expands the phenotypic spectrum of early onset SCA2 and points out the importance of considering SCA2 gene analysis in children with progressive neurological impairment and abnormal movements with or without polyphagia.]. 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:18297329;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP657165.RAY-zyP0qMLfONO7Aowk4aqplFHcBKa8xZB0LLlYpzTek130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:43+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: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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}