@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg> .
@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:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_head {
  this: np:hasAssertion dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_assertion;
    np:hasProvenance dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_provenance;
    np:hasPublicationInfo dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_assertion a np:Assertion .
  
  dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_provenance a np:Provenance .
  
  dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_assertion {
  miriam-gene:127 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN57fee924cf4d3fe002f90a9d6e8ab253 sio:SIO_000628 miriam-gene:127, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_provenance {
  dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_assertion dcterms:description
      "[an association between a certain ADH4 (formerly known as ADH7 in humans) allele and PD. This suggests a role for genetic variations of ADH4 as risk factors for the development of PD. Our data also show that the observed polymorphisms alone are not sufficient to cause symptoms. Further genetic and/or environmental factors have to be involved.]. 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:11009184;
    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:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}