@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA> .
@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/v3.0.0/void/> .

dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_head {
  this: np:hasAssertion dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_assertion;
    np:hasProvenance dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_provenance;
    np:hasPublicationInfo dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_assertion a np:Assertion .
  
  dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_provenance a np:Provenance .
  
  dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_assertion {
  miriam-gene:9937 a ncit:C16612 .
  
  lld:C0002871 a ncit:C7057 .
  
  dgn-gda:DGN4d43403bfa6067d3d352862ee38dcd7c sio:SIO_000628 miriam-gene:9937, lld:C0002871;
    a sio:SIO_001121 .
}

dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_provenance {
  dgn-np:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_assertion dcterms:description
      "[In their sensitivity only to difunctional compounds and lack of an apparent DNA excision repair defect the phenotype of Walker cells strongly resembles those cells from human patients suffering from Fanconi's anaemia and also of yeast snm1 mutant cells.]. 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:1719394;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP832695.RAtZsmmdkDhE9KZaFdnxMrP2UDyGwsNsAarzp8Lur9yiA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:05+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}