@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts> .
@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:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_head {
  this: np:hasAssertion dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_assertion ;
    np:hasProvenance dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_provenance ;
    np:hasPublicationInfo dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_assertion a np:Assertion .
  dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_provenance a np:Provenance .
  dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_assertion {
  miriam-gene:4210 a ncit:C16612 .
  lld:C0035435 a ncit:C7057 .
  dgn-gda:DGNf188ac9c0e3d1a523771561c1e47c5bc sio:SIO_000628 miriam-gene:4210 , lld:C0035435 ;
    a sio:SIO_001121 .
}
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_provenance {
  dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_assertion dcterms:description "[These findings suggest that mutations of the MEFV gene may be responsible for rheumatic diseases other than FMF, and patients with JIA especially males, ANA negatives, and ERA subgroups should be screened for MEFV gene mutations in countries where FMF is frequent.]. 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:23588594 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:07+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" .
}