@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM> .
@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:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_head {
   this: np:hasAssertion dgn-np:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_assertion ;
    np:hasProvenance dgn-np:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_provenance ;
    np:hasPublicationInfo dgn-np:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_assertion a np:Assertion .
  dgn-np:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_provenance a np:Provenance .
  dgn-np:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_assertion {
   miriam-gene:4889 a ncit:C16612 .
  lld:C0020179 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_provenance {
   dgn-np:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_assertion dcterms:description "[Therefore, the aim of the present study was to analyze different single nucleotide polymorphisms (SNPs) in order to test the possibility that genetic variation in NPY or three of its receptor genes (NPY1R, NPY2R, and NPY5R) may explain some of the variation in AO of HD motor manifestations, in a comprehensive cohort of 487 German HD patients.]. 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:24121255 ;
    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:NP1118631.RAo39IWnrK52h6jgIkmcPtDRrze03jEdKyb0HumuXCbCM130_publicationInfo {
   this: dcterms:created "2016-05-13T12:50:13+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" .
}