@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0> .
@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:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_head {
   this: np:hasAssertion dgn-np:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_assertion ;
    np:hasProvenance dgn-np:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_provenance ;
    np:hasPublicationInfo dgn-np:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_assertion a np:Assertion .
  dgn-np:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_provenance a np:Provenance .
  dgn-np:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_assertion {
   miriam-gene:367 a ncit:C16612 .
  lld:C0087012 a ncit:C7057 .
  dgn-gda:DGNcf25db5b387ebffb9a55bafe9386998b sio:SIO_000628 miriam-gene:367 , lld:C0087012 ;
    a sio:SIO_001121 .
}
dgn-np:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_provenance {
   dgn-np:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_assertion dcterms:description "[To date, eight neurodegenerative diseases, including Huntington's disease, dentatorubral-pallidoluysian atrophy, spinal and bulbar muscular atrophy, and spinocerebellar ataxia (SCA) types 1, 2, 3, 6, and 7, have been proven to be caused by an expanded trinucleotide repeat (CAG)n located within a specific gene for each of these diseases.]. 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:9836074 ;
    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:NP556830.RAwbZsSbVjGI2j2ZGC1wwWTo94s4jHnp2N-l2oiQ7ebM0130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:35+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" .
}