@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4> .
@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:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_head {
  this: np:hasAssertion dgn-np:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_assertion;
    np:hasProvenance dgn-np:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_provenance;
    np:hasPublicationInfo dgn-np:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_assertion a np:Assertion .
  
  dgn-np:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_provenance a np:Provenance .
  
  dgn-np:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_assertion {
  miriam-gene:2837 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGN98673408db7176dfab964a80cf321a7b sio:SIO_000628 miriam-gene:2837, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_provenance {
  dgn-np:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_assertion dcterms:description
      "[We have tested this hypothesis by sequencing all GRIK2 exons, the exon-flanking sequences and 3'UTR in several individuals who were crucial to demonstrating the modifier effect, as they showed much earlier age at neurological onset than would be expected from the length of their HD CAG mutation.]. 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:16959037;
    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:NP806577.RATTagadFjvKOxaEwbxDFPe61iwCOO4e7XQrzU7OUg5Z4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:14+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" .
}