@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4> .
@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:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_head {
  this: np:hasAssertion dgn-np:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_assertion;
    np:hasProvenance dgn-np:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_provenance;
    np:hasPublicationInfo dgn-np:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_assertion a np:Assertion .
  
  dgn-np:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_provenance a np:Provenance .
  
  dgn-np:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_assertion {
  miriam-gene:7132 a ncit:C16612 .
  
  lld:C0847014 a ncit:C7057 .
  
  dgn-gda:DGN9a60bd2055c855ba77689a0fb1664ab5 sio:SIO_000628 miriam-gene:7132, lld:C0847014;
    a sio:SIO_001121 .
}

dgn-np:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_provenance {
  dgn-np:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_assertion dcterms:description
      "[Among them it is recognized the TNF receptor associated periodic syndrome (TRAPS) caused by mutations in the TNFRSF1A gene and characterized by symptoms such as recurrent high fevers, rash, abdominal pain, arthralgia and myalgia.]. 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:21567205;
    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:NP266180.RAhQF3yw7N_M1uWOK75ENow_qgMw46eP5BS1c05X4dhN4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}