@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs> .
@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:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_head {
  this: np:hasAssertion dgn-np:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_assertion;
    np:hasProvenance dgn-np:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_provenance;
    np:hasPublicationInfo dgn-np:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_assertion a np:Assertion .
  
  dgn-np:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_provenance a np:Provenance .
  
  dgn-np:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_assertion {
  miriam-gene:4049 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN81af9338a1819dc9e11b213403e9dd60 sio:SIO_000628 miriam-gene:4049, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_provenance {
  dgn-np:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_assertion dcterms:description
      "[Our data suggest an effect of the TNFalpha-308 polymorphism on the age at onset of late AD. This represents additional evidence of the importance of genetic variation at the proinflammatory components in the origin and progression of this common NEUROLOGICALenerative disease.]. 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:12116197;
    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:NP55132.RAWTK_4BDhHLhdbB5-qWad1-4K0STMAbJjzI6cV49NKTs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}