@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c> .
@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:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_head {
  this: np:hasAssertion dgn-np:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_assertion ;
    np:hasProvenance dgn-np:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_provenance ;
    np:hasPublicationInfo dgn-np:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_assertion a np:Assertion .
  dgn-np:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_provenance a np:Provenance .
  dgn-np:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_assertion {
  miriam-gene:4210 a ncit:C16612 .
  lld:C0585274 a ncit:C7057 .
  dgn-gda:DGN3c9a3ea35b29b31c7a2a7337142001ad sio:SIO_000628 miriam-gene:4210 , lld:C0585274 ;
    a sio:SIO_001121 .
}
dgn-np:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_provenance {
  dgn-np:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_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:NP683763.RAIO5ahUWOrhn8WyWRvQ4xG2iL2sNMTEMXbzqo17YVw8c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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> ;
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