@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8> .
@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:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_head {
  this: np:hasAssertion dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_assertion ;
    np:hasProvenance dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_provenance ;
    np:hasPublicationInfo dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_assertion a np:Assertion .
  dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_provenance a np:Provenance .
  dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  lld:C0085390 a ncit:C7057 .
  dgn-gda:DGNbe8923aad710086da97e405040531d8e sio:SIO_000628 miriam-gene:3342 , lld:C0085390 ;
    a sio:SIO_001121 .
}
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_provenance {
  dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_assertion dcterms:description "[Studies of Li-Fraumeni syndrome fibroblasts heterozygous for germline TP53 mutations have shown that loss of heterozygosity (LOH) occurs during passaging and is associated with genomic instability, such as chromosomal aberrations and aneuploidy to investigate the genomic changes associated with LOH in Li-Fraumeni (LF) fibroblasts, we have analysed cell strains at increasing population doublings (PD) using Comparative Genomic Hybridization (CGH).]. 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:10945493 ;
    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:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:10+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" .
}