@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_head {
  this: np:hasAssertion dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_assertion;
    np:hasProvenance dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_provenance;
    np:hasPublicationInfo dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_assertion a np:Assertion .
  
  dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_provenance a np:Provenance .
  
  dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_assertion {
  miriam-gene:64127 a ncit:C16612 .
  
  lld:C0039082 a ncit:C7057 .
  
  dgn-gda:DGN600552c5d6257412910b93f5b6a6904d sio:SIO_000628 miriam-gene:64127, lld:C0039082;
    a sio:SIO_001122 .
}

dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_provenance {
  dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_assertion dcterms:description
      "[Danish sarcoidosis patients have frequent variations in CARD15 exon 4, but do not present any mutation associated with Blau syndrome. The variations found had no influence on the course of 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:20298285;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:36+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}