@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U> .
@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:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_head {
  this: np:hasAssertion dgn-np:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_assertion;
    np:hasProvenance dgn-np:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_provenance;
    np:hasPublicationInfo dgn-np:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_assertion a np:Assertion .
  
  dgn-np:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_provenance a np:Provenance .
  
  dgn-np:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_assertion {
  miriam-gene:4790 a ncit:C16612 .
  
  lld:C0011854 a ncit:C7057 .
  
  dgn-gda:DGN5987bf85748e047f952a43852b9aa6ce sio:SIO_000628 miriam-gene:4790, lld:C0011854;
    a sio:SIO_001121 .
}

dgn-np:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_provenance {
  dgn-np:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_assertion dcterms:description
      "[The M55V substitution of SUMO4 may affect its ability to modify IκBα by sumoylation, and so lead to activation of NFκB and transcription of genes implicated in the development of type 1 diabetes.]. 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:22069273;
    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:NP528265.RA6xpAclGVxaYSOw62VxMuQ81q1NgOCsg7szeWSFtbY7U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:19+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" .
}