@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU> .
@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:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_head {
  this: np:hasAssertion dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_assertion ;
    np:hasProvenance dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_provenance ;
    np:hasPublicationInfo dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_assertion a np:Assertion .
  dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_provenance a np:Provenance .
  dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_assertion {
  miriam-gene:4210 a ncit:C16612 .
  lld:C0031069 a ncit:C7057 .
  dgn-gda:DGNe06207d49735beac628218f864b4d81f sio:SIO_000628 miriam-gene:4210 , lld:C0031069 ;
    a sio:SIO_001122 .
}
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_provenance {
  dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_assertion dcterms:description "[To assess the protective as well as the modulating affect of MEFV mutation carriage on various inflammatory disease states, we sought to define the frequency of MEFV mutations in Israeli Jewish individuals of various ethnicities, including those with low frequency of FMF, which were not in the focus of our attention hitherto.]. 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:19373257 ;
    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:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_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" .
}