@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY> .
@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:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_head {
  this: np:hasAssertion dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_assertion ;
    np:hasProvenance dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_provenance ;
    np:hasPublicationInfo dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_assertion a np:Assertion .
  dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_provenance a np:Provenance .
  dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_assertion {
  miriam-gene:9051 a ncit:C16612 .
  lld:C1692886 a ncit:C7057 .
  dgn-gda:DGNf31ae4d3d37cdd9bdf34d215d523188a sio:SIO_000628 miriam-gene:9051 , lld:C1692886 ;
    a sio:SIO_001121 .
}
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_provenance {
  dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_assertion dcterms:description "[Although common features of human PAPA syndrome such as pyogenic arthritis and skin inflammation were not recapitulated in the mouse model, ectopic expression of the mutant but not the wild type PSTPIP1 in mice lead to partial embryonic lethality, growth retardation, and elevated level of circulating proinflammatory cytokines.]. 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:23293022 ;
    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:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:10+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" .
}