@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk> .
@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:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_head {
  this: np:hasAssertion dgn-np:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_assertion;
    np:hasProvenance dgn-np:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_provenance;
    np:hasPublicationInfo dgn-np:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_assertion a np:Assertion .
  
  dgn-np:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_provenance a np:Provenance .
  
  dgn-np:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_assertion {
  miriam-gene:9051 a ncit:C16612 .
  
  lld:C0011603 a ncit:C7057 .
  
  dgn-gda:DGNc13255a4dc2943c2487a06deae13a691 sio:SIO_000628 miriam-gene:9051, lld:C0011603;
    a sio:SIO_001121 .
}

dgn-np:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_provenance {
  dgn-np:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_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:NP257418.RA-pt-yuTNYk7sVIcIsxMZMSthfGl9NGw8JzyOakmbogk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}