@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs> .
@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:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_head {
  this: np:hasAssertion dgn-np:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_assertion;
    np:hasProvenance dgn-np:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_provenance;
    np:hasPublicationInfo dgn-np:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_assertion a np:Assertion .
  
  dgn-np:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_provenance a np:Provenance .
  
  dgn-np:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGN7289ae4d9a3dbafa6c1b8e343d9097aa sio:SIO_000628 miriam-gene:367, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_provenance {
  dgn-np:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_assertion dcterms:description
      "[Our results indicate that in SBMA, in contrast to sperm typing analysis of Huntington's disease, there is relative stability of the CAG repeat number during paternal transmissions and that the spectrum of mutations is narrow.]. 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:10732798;
    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:NP451206.RACxFfxgm48LaJf6YqL_ttgapWsNM33P1MZEt4vTBsEIs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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" .
}