@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo> .
@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:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_head {
  this: np:hasAssertion dgn-np:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_assertion;
    np:hasProvenance dgn-np:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_provenance;
    np:hasPublicationInfo dgn-np:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_assertion a np:Assertion .
  
  dgn-np:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_provenance a np:Provenance .
  
  dgn-np:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_assertion {
  miriam-gene:83882 a ncit:C16612 .
  
  lld:C0333559 a ncit:C7057 .
  
  dgn-gda:DGN95fb45901d112470f229d8a8ca8d367b sio:SIO_000628 miriam-gene:83882, lld:C0333559;
    a sio:SIO_001121 .
}

dgn-np:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_provenance {
  dgn-np:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_assertion dcterms:description
      "[When patients were categorized according to the OCSP classification, it turned out that significant (p=0.002) decrease in TNF2 allele frequency (0.065) was restricted to the patients with lacunar infarct (LACI) whereas the frequency of the TNF2 alleles in patients with the other three subtypes (TACI, PACI, and POCI) did not significantly differ from that in 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:16473522;
    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:NP169329.RAGHqPMkcOcRc5pJK2ouI17rambTF_gZgwKW7KTTOAzeo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}