@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA> .
@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 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:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_head {
  this: np:hasAssertion dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_assertion;
    np:hasProvenance dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_provenance;
    np:hasPublicationInfo dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_assertion a np:Assertion .
  
  dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_provenance a np:Provenance .
  
  dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_assertion {
  miriam-gene:338340 a ncit:C16612 .
  
  lld:C0017097 a ncit:C7057 .
  
  dgn-gda:DGN5d2685b4cc12e0f9006a6272a4d7d5c8 sio:SIO_000628 miriam-gene:338340, lld:C0017097;
    a sio:SIO_001121 .
}

dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_provenance {
  dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_assertion dct:description
      "[Fibroblasts from the clinically affected Gardner's syndrome daughter of the proband were significantly more sensitive to MMS treatment, D0 of 0.22 mM (p less than 0.01) versus the normal average D0 of 0.36 mM and a D10 of 0.97 mM (p less than 0.01) versus the normal average.]. 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:6800649;
    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:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_publicationInfo {
  this: dct:created "2014-10-02T12:33:48+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}