@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA> .
@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 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:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_head {
  this: np:hasAssertion dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_assertion;
    np:hasProvenance dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_provenance;
    np:hasPublicationInfo dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_assertion a np:Assertion .
  
  dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_provenance a np:Provenance .
  
  dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_assertion {
  miriam-gene:727 a ncit:C16612 .
  
  lld:C0035439 a ncit:C7057 .
  
  dgn-gda:DGN106ff1dcf1fbc874a1195ffe71e22d9b sio:SIO_000628 miriam-gene:727, lld:C0035439;
    a sio:SIO_001122 .
}

dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_provenance {
  dgn-np:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_assertion dc:description
      "[We observed no association with RHD for the five tagging single nucleotide polymorphisms (tSNP) in the C5 gene, the three tSNPs in the TNFAIP3 gene, or the two tSNPs in the TRAF1 gene.]. 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:19902201;
    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:NP79588.RAbRLtKTy6AJT0bIT_T0kyxZZJCP5jOe_XyEiu8uCgNaA130_publicationInfo {
  this: dc:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}