@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY> .
@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:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_head {
  this: np:hasAssertion dgn-np:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_assertion ;
    np:hasProvenance dgn-np:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_provenance ;
    np:hasPublicationInfo dgn-np:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_assertion a np:Assertion .
  dgn-np:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_provenance a np:Provenance .
  dgn-np:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_assertion {
  miriam-gene:641 a ncit:C16612 .
  lld:C0004135 a ncit:C7057 .
  dgn-gda:DGN035a72568d7c7669116e508e819e20c2 sio:SIO_000628 miriam-gene:641 , lld:C0004135 ;
    a sio:SIO_001121 .
}
dgn-np:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_provenance {
  dgn-np:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_assertion dcterms:description "[We also discuss how this model of H2AX function could account for some aspects of the genomic instability and cancer prone human phenotypes associated with Ataxia Telangiectasia (AT), Nijmegen Breakage Syndrome (NBS), Ataxia Telangiectasia Like Disorder (ATLD), and Bloom's Syndrome (BS).]. 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:14712078 ;
    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:NP605005.RAP20vLwwWQP3yHcIwSdRHschRTCUkX58g0Xo2tC0KfWY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:03+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" .
}