@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA> .
@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:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_head {
  this: np:hasAssertion dgn-np:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_assertion;
    np:hasProvenance dgn-np:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_provenance;
    np:hasPublicationInfo dgn-np:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_assertion a np:Assertion .
  
  dgn-np:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_provenance a np:Provenance .
  
  dgn-np:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_assertion {
  miriam-gene:5444 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGN197d0ed49da5b50039eeaf1708b4fa55 sio:SIO_000628 miriam-gene:5444, lld:C0002736;
    a sio:SIO_001121 .
}

dgn-np:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_provenance {
  dgn-np:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_assertion dcterms:description
      "[Due to a reported possible twofold increased risk of ALS in Gulf War veterans and the associations of PON1 polymorphisms with the neurologic symptom complex of the Gulf War syndrome, the authors investigated the association between sporadic ALS (SALS) and PON gene cluster variants in a large North American Caucasian family-based and case-control cohort (N = 1,891).]. 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:16822964;
    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:NP617652.RAiL8sr9K9bcxjc1JnWx6I3wrwptust8IbtXYaVB8OAJA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:13+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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}