@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8> .
@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:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_head {
  this: np:hasAssertion dgn-np:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_assertion ;
    np:hasProvenance dgn-np:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_provenance ;
    np:hasPublicationInfo dgn-np:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_assertion a np:Assertion .
  dgn-np:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_provenance a np:Provenance .
  dgn-np:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_assertion {
  miriam-gene:80055 a ncit:C16612 .
  lld:C0030567 a ncit:C7057 .
  dgn-gda:DGN83658e33e821110284e1251e13810391 sio:SIO_000628 miriam-gene:80055 , lld:C0030567 ;
    a sio:SIO_001121 .
}
dgn-np:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_provenance {
  dgn-np:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_assertion dcterms:description "[Subgroup analysis by ethnicity showed significantly stronger effects for the BST1 (rs11724635) in Asian vs Caucasian populations and similar effects for SNCA, LRRK2, LAMP3, HIP1R, and STK39 in Asian and Caucasian populations, while MAPT rs2942168 and SYT11 rs34372695 were monomorphic in the Asian population, highlighting the role of population-specific heterogeneity in PD.]. 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:22786590 ;
    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:NP428068.RAAt97P88RBE2TvCieHmtXLVE2IXk_dmDCxaZeEk0opY8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:13+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: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> ;
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