@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_head {
   this: np:hasAssertion dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_assertion ;
    np:hasProvenance dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_provenance ;
    np:hasPublicationInfo dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_assertion a np:Assertion .
  dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_provenance a np:Provenance .
  dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_assertion {
   miriam-gene:7349 a ncit:C16612 .
  lld:C3469521 a ncit:C7057 .
  dgn-gda:DGN13f5282bb2148b63045c2fe4f83c1b7d sio:SIO_000628 miriam-gene:7349 , lld:C3469521 ;
    a sio:SIO_001121 .
}
dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_provenance {
   dgn-np:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_assertion dcterms:description "[Using isogenic pairs of cell lines differing only in the Fanconi Anemia (FA) DNA repair pathway, we showed that FA deficient cell lines were hypersensitive to CHK1 silencing by independent siRNAs as well as CHK1 pharmacologic inhibition by Gö6976 and UCN-01.]. 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:19371427 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP732730.RAPv5x73JXMD3HfrxzudxH440jbgAc7fsJ0XQ6RHddRhM130_publicationInfo {
   this: dcterms:created "2016-05-13T12:47:17+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}