@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI> .
@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:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_head {
  this: np:hasAssertion dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_assertion;
    np:hasProvenance dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_provenance;
    np:hasPublicationInfo dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_assertion a np:Assertion .
  
  dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_provenance a np:Provenance .
  
  dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_assertion {
  miriam-gene:4210 a ncit:C16612 .
  
  lld:C0031069 a ncit:C7057 .
  
  dgn-gda:DGN706a697d87a9bbd41f08327eccf3831e sio:SIO_000628 miriam-gene:4210, lld:C0031069;
    a sio:SIO_001122 .
}

dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_provenance {
  dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_assertion dcterms:description
      "[A total of 19 FMF patients and eight healthy individuals were genotyped for mutations in the MEFV gene and gut bacterial diversity was assessed by sequencing 16S rRNA gene libraries and FISH analysis.]. 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:18725973;
    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:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_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" .
}