@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM> .
@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:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_head {
  this: np:hasAssertion dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_assertion ;
    np:hasProvenance dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_provenance ;
    np:hasPublicationInfo dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_assertion a np:Assertion .
  dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_provenance a np:Provenance .
  dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_assertion {
  miriam-gene:23038 a ncit:C16612 .
  lld:C1863239 a ncit:C7057 .
  dgn-gda:DGNcccaa0ae89030e2072712af8c1f630e0 sio:SIO_000628 miriam-gene:23038 , lld:C1863239 ;
    a sio:SIO_001121 .
}
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_provenance {
  dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_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:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:28+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" .
}