@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM> .
@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:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_head {
  this: np:hasAssertion dgn-np:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_assertion ;
    np:hasProvenance dgn-np:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_provenance ;
    np:hasPublicationInfo dgn-np:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_assertion a np:Assertion .
  dgn-np:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_provenance a np:Provenance .
  dgn-np:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_assertion {
  miriam-gene:4069 a ncit:C16612 .
  lld:C0585274 a ncit:C7057 .
  dgn-gda:DGN86a1f15c9b2a47402172c8e525b5ae1d sio:SIO_000628 miriam-gene:4069 , lld:C0585274 ;
    a sio:SIO_001121 .
}
dgn-np:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_provenance {
  dgn-np:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_assertion dcterms:description "[Among hereditary fevers characterized by recurrent attacks of fever and organ localized inflammation, familial Mediterranean fever (FMF), and tumour necrosis factor receptor superfamily 1A (TNFRSF1A) receptor associated periodic syndrome (TRAPS) are diseases with identified genes that can be associated with renal amyloidosis of the AA type.]. 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:12105243 ;
    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:NP707184.RA0dniCWn2zsLgVXUu_zxWegObc5Yykkq6xcBEYyQl0ZM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:09+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" .
}