@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs> .
@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:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_head {
  this: np:hasAssertion dgn-np:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_assertion ;
    np:hasProvenance dgn-np:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_provenance ;
    np:hasPublicationInfo dgn-np:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_assertion a np:Assertion .
  dgn-np:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_provenance a np:Provenance .
  dgn-np:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  lld:C0030567 a ncit:C7057 .
  dgn-gda:DGNe4532f2a320d917e8f548e6a8c3fc168 sio:SIO_000628 miriam-gene:4846 , lld:C0030567 ;
    a sio:SIO_001122 .
}
dgn-np:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_provenance {
  dgn-np:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_assertion dcterms:description "[Coding and tagging single nucleotide polymorphisms (SNPs) (27 NOS1, 18 NOS2A, and five NOS3 SNPs) were genotyped in families with PD (1,065 cases and 1,180 relative and other controls) and were tested for allelic associations with PD using the association in the presence of linkage test and the pedigree disequilibrium test (PDT), allelic associations with age-at-onset (AAO) using the quantitative transmission disequilibrium test, and interactions using the multifactor dimensionality reduction-PDT.]. 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:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP68946.RA26ppKdizb8lQcT0mG-7Vi1DqDMxcQlPbUPqDt83HHqs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:33+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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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}