@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4> .
@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:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_head {
  this: np:hasAssertion dgn-np:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_assertion ;
    np:hasProvenance dgn-np:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_provenance ;
    np:hasPublicationInfo dgn-np:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_provenance a np:Provenance .
  dgn-np:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_assertion {
  miriam-gene:11186 a ncit:C16612 .
  lld:C0005695 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_provenance {
  dgn-np:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_assertion dcterms:description "[Moreover, both tumors exhibited an identical mutation in p53, as well as similar loss of heterozygosity at 10q23 and RASSF1A promoter hypermethylation, clearly indicating that the bladder tumor was the site for the primary tumor of the patient.]. 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:18446450 ;
    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:NP413650.RAmgZsjlI_6mpB5pl1RRV1uaz96WuWZ-fnQ8kc7kQPfo4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:05+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}