@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU> .
@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:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_head {
  this: np:hasAssertion dgn-np:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_assertion ;
    np:hasProvenance dgn-np:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_provenance ;
    np:hasPublicationInfo dgn-np:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_assertion a np:Assertion .
  dgn-np:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_provenance a np:Provenance .
  dgn-np:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_assertion {
  miriam-gene:4135 a ncit:C16612 .
  lld:C0009402 a ncit:C7057 .
  dgn-gda:DGN53dc61a4d11337c7479f1aafb7f474dd sio:SIO_000628 miriam-gene:4135 , lld:C0009402 ;
    a sio:SIO_001121 .
}
dgn-np:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_provenance {
  dgn-np:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_assertion dcterms:description "[The cases studied were five colorectal carcinomas, two specimens of normal colorectal mucosa, and four colorectal carcinomas with genetic alterations which are expected to preclude p53 gene product expression, namely mutation to a STOP codon in the p53 gene detected by denaturing gradient gel electrophoresis with subsequent sequencing and allelic loss of 17p in the region where p53 is located, detected by restriction fragment length polymorphism analysis.]. 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:8778330 ;
    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:NP661834.RA6Lyh2LmrztlNgzITMAbd6navAQEq4bPL5u0HnzzIyZU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:40+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" .
}