@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc> .
@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:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_head {
  this: np:hasAssertion dgn-np:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_assertion;
    np:hasProvenance dgn-np:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_provenance;
    np:hasPublicationInfo dgn-np:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_assertion a np:Assertion .
  
  dgn-np:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_provenance a np:Provenance .
  
  dgn-np:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_assertion {
  miriam-gene:55239 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGNc9fcc077b9aaeeb75f14cbf4630d7fa9 sio:SIO_000628 miriam-gene:55239, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_provenance {
  dgn-np:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_assertion dcterms:description
      "[We identified novel moderately rare variants in several genes, including SCAPER, HYDIN, UBE2H, EZR, MMRN2 and OGFOD1 that were specifically present in PD patients or enriched among them, nominating these as novel candidate risk genes for PD, although no variants achieved genome-wide significance after Bonferroni correction.]. 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:25294124;
    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:NP1227154.RA7GPXpXe48R5x0dtybgS2vjxV8WyJWE7-uYnb4lY7ZZc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:02+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" .
}