@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0> .
@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:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_head {
  this: np:hasAssertion dgn-np:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_assertion;
    np:hasProvenance dgn-np:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_provenance;
    np:hasPublicationInfo dgn-np:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_assertion a np:Assertion .
  
  dgn-np:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_provenance a np:Provenance .
  
  dgn-np:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_assertion {
  miriam-gene:2194 a ncit:C16612 .
  
  lld:C1328840 a ncit:C7057 .
  
  dgn-gda:DGN938c758f40c7dbb16a26fbadeb75b9f0 sio:SIO_000628 miriam-gene:2194, lld:C1328840;
    a sio:SIO_001121 .
}

dgn-np:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_provenance {
  dgn-np:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_assertion dcterms:description
      "[Patients have been identified with defects affecting the extrinsic apoptotic pathway mediated by the protein receptor FAS which results in the autoimmune lymphoproliferative syndrome and more recently in defects affecting the intrinsic apoptotic pathway mediated by RAS proteins resulting in the RAS-associated autoimmune leukoproliferative disorder.]. 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:22918222;
    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:NP468924.RAAG6Z6pbJFZxXY7MIO9Wnq6Oihv0RkEf6CabvA2SdNe0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:41+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" .
}