@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg> .
@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:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_head {
  this: np:hasAssertion dgn-np:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_assertion;
    np:hasProvenance dgn-np:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_provenance;
    np:hasPublicationInfo dgn-np:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_assertion a np:Assertion .
  
  dgn-np:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_provenance a np:Provenance .
  
  dgn-np:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_assertion {
  miriam-gene:4210 a ncit:C16612 .
  
  lld:C0751422 a ncit:C7057 .
  
  dgn-gda:DGN89780e5c5c761370666d923c6289e908 sio:SIO_000628 miriam-gene:4210, lld:C0751422;
    a sio:SIO_001121 .
}

dgn-np:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_provenance {
  dgn-np:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_assertion dcterms:description
      "[The high percentage (66.61%) of patients with unidentified mutations could be due to mutations in the rest of the coding or noncoding MEFV gene or due to mutations in other genes that are also causing Hereditary Recurrent Fevers.]. 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:25393764;
    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:NP1237149.RACfAv78a8TeWR96b5UK1ooMzDPUsAv5z-cIf6fXcE8Jg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:06+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" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}