@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8> .
@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:NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8130_head {
  this: np:hasAssertion dgn-np:NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8130_assertion ;
    np:hasProvenance dgn-np:NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8130_provenance ;
    np:hasPublicationInfo dgn-np:NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8130_assertion {
  miriam-gene:4487 a ncit:C16612 .
  lld:C0020179 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8130_provenance {
  dgn-np:NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8130_assertion dcterms:description "[We used data from 535 HD participants of the New England Huntington cohort and the HD MAPS cohort to assess whether AO was influenced by any of the three markers in the 4p16 region: MSX1 (Drosophila homeo box homologue 1, formerly known as homeo box 7, HOX7), Delta2642 (within the HD coding sequence), and BJ56 ( D4S127).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP476488.RAcXIjrfbfDrYkV8qGmni2nKOIRgyRNts2SsUL1B-J2F8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:45+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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