@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY> .
@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:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_head {
  this: np:hasAssertion dgn-np:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_assertion;
    np:hasProvenance dgn-np:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_provenance;
    np:hasPublicationInfo dgn-np:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_assertion a np:Assertion .
  
  dgn-np:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_provenance a np:Provenance .
  
  dgn-np:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_assertion {
  miriam-gene:3064 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGN6749a7fb5a5b98a046a1c0fe9d742094 sio:SIO_000628 miriam-gene:3064, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_provenance {
  dgn-np:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_assertion dcterms:description
      "[Unintended weight loss, sleep and circadian disturbances and autonomic dysfunction are prevalent features of Huntington's disease (HD), an autosomal dominantly inherited neurodegenerative disorder caused by an expanded CAG repeat sequence in the HTT gene.]. 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:25074766;
    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:NP1206224.RAHVnHNRlsVakM9bzn6dXi5LM4ONX4D7Mm0qP28KIA9QY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:52+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" .
}