@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc> .
@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:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_head {
  this: np:hasAssertion dgn-np:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_assertion ;
    np:hasProvenance dgn-np:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_provenance ;
    np:hasPublicationInfo dgn-np:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_assertion a np:Assertion .
  dgn-np:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_provenance a np:Provenance .
  dgn-np:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_assertion {
  miriam-gene:23038 a ncit:C16612 .
  lld:C0268124 a ncit:C7057 .
  dgn-gda:DGN7fa3a4487a9c9844d00ec18fa3407696 sio:SIO_000628 miriam-gene:23038 , lld:C0268124 ;
    a sio:SIO_001121 .
}
dgn-np:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_provenance {
  dgn-np:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_assertion dcterms:description "[Excessive poly(ADP-ribose) synthesis, provoked by DNA strand breakage, may represent a common pathway that connects the immunodeficiency syndromes associated with (a) exposure of lymphocytes to toxic oxygen species during chronic inflammatory states, (b) adenosine deaminase deficiency, and (c) certain DNA repair disorders.]. 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:3950545 ;
    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:NP556498.RAfJVbgawTWK4DJ0BEl68fdsM0cOuaPNuLdmdLj2LvTxc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:35+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" .
}