@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c> .
@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:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_head {
  this: np:hasAssertion dgn-np:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_assertion;
    np:hasProvenance dgn-np:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_provenance;
    np:hasPublicationInfo dgn-np:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_assertion a np:Assertion .
  
  dgn-np:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_provenance a np:Provenance .
  
  dgn-np:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_assertion {
  miriam-gene:5599 a ncit:C16612 .
  
  lld:C3489791 a ncit:C7057 .
  
  dgn-gda:DGN66ae25d3db3464b1ea129b5abc11e6a9 sio:SIO_000628 miriam-gene:5599, lld:C3489791;
    a sio:SIO_001121 .
}

dgn-np:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_provenance {
  dgn-np:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_assertion dcterms:description
      "[We therefore compared total levels and activation of the signalling proteins Src, HSP27, p38 MAPK, JNK, and ERK, in extracts of leukocytes isolated from patients with PD carrying the G2019S mutation, healthy mutation carriers, patients with idiopathic PD, and healthy controls.]. 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:17385669;
    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:NP504635.RABxV_zS0L8cDGqFh_pRK5jLxMv59JH_UXkHO3JC8Jk1c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:00+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" .
}