@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ> .
@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:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_head {
  this: np:hasAssertion dgn-np:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_assertion;
    np:hasProvenance dgn-np:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_provenance;
    np:hasPublicationInfo dgn-np:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_assertion a np:Assertion .
  
  dgn-np:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_provenance a np:Provenance .
  
  dgn-np:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_assertion {
  miriam-gene:64127 a ncit:C16612 .
  
  lld:C0042164 a ncit:C7057 .
  
  dgn-gda:DGNa81c56f26d6228eb7db72052ae116398 sio:SIO_000628 miriam-gene:64127, lld:C0042164;
    a sio:SIO_001121 .
}

dgn-np:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_provenance {
  dgn-np:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_assertion dcterms:description
      "[Blau's syndrome (familial juvenile systemic granulomatosis) presents with non-caseating granulomatous inflammation affecting the joint, skin, and uveal tract (the triad of arthritis, dermatitis and uveitis) and is associated with mutations of the NACHT domain of the gene CARD15 (or NOD2).]. 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:22714396;
    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:NP461801.RAC4MGH8O3cEOM7M6emOGr4la3qdclLq2Yu1X07AIjQfQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:35+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" .
}