@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM> .
@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:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_head {
  this: np:hasAssertion dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_assertion ;
    np:hasProvenance dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_provenance ;
    np:hasPublicationInfo dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_assertion a np:Assertion .
  dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_provenance a np:Provenance .
  dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_assertion {
  miriam-gene:7124 a ncit:C16612 .
  lld:C0031069 a ncit:C7057 .
  dgn-gda:DGNec9737c6807d09825763fc1d3b6519b2 sio:SIO_000628 miriam-gene:7124 , lld:C0031069 ;
    a sio:SIO_001121 .
}
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_provenance {
  dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_assertion dcterms:description "[Abstract A host of clinical scenarios can be depicted in hereditary autoinflammatory diseases, and the cardiovascular system can also be involved especially in familial Mediterranean fever (FMF), caused by mutations in the MEFV gene, and tumour necrosis factor receptor-associated periodic syndrome (TRAPS), caused by mutations in the TNFRSF1A gene.]. 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:21284530 ;
    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:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:32+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" .
}