@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo> .
@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/v4.0.0/void/> .
dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_head {
   this: np:hasAssertion dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_assertion ;
    np:hasProvenance dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_provenance ;
    np:hasPublicationInfo dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_assertion a np:Assertion .
  dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_provenance a np:Provenance .
  dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_assertion {
   miriam-gene:114548 a ncit:C16612 .
  lld:C0003873 a ncit:C7057 .
  dgn-gda:DGN043480ba2e9c4c592d0ce0112ea3a716 sio:SIO_000628 miriam-gene:114548 , lld:C0003873 ;
    a sio:SIO_001121 .
}
dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_provenance {
   dgn-np:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_assertion dcterms:description "[We investigated the hypothesis that low-penetrance mutations in genes (TNFRSF1A, MEFV and NALP3/CIAS1) associated with hereditary periodic fever syndromes (HPFs) might be risk factors for AA amyloidosis among patients with chronic inflammatory disorders, including rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), Crohn's disease, undiagnosed recurrent fevers and HPFs themselves.]. 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:15071491 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP439041.RAaRwX32o1Ndzg2OZdo9XIMms_acLnX3c_u18cTn0mRBo130_publicationInfo {
   this: dcterms:created "2016-05-13T12:45:04+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 "v4.0.0.0" .
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}