@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1369146.RANoNP3dpUx5ChKyjpKyPNCgoKPpKWz-aw9Jtd1uVG0aM> .
@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/v4.0.0/void/> .

dgn-np:NP1369146.RANoNP3dpUx5ChKyjpKyPNCgoKPpKWz-aw9Jtd1uVG0aM130_head {
  this: np:hasAssertion dgn-np:NP1369146.RANoNP3dpUx5ChKyjpKyPNCgoKPpKWz-aw9Jtd1uVG0aM130_assertion;
    np:hasProvenance dgn-np:NP1369146.RANoNP3dpUx5ChKyjpKyPNCgoKPpKWz-aw9Jtd1uVG0aM130_provenance;
    np:hasPublicationInfo dgn-np:NP1369146.RANoNP3dpUx5ChKyjpKyPNCgoKPpKWz-aw9Jtd1uVG0aM130_publicationInfo;
    a np:Nanopublication .
  
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    a np:PublicationInfo .
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dgn-np:NP1369146.RANoNP3dpUx5ChKyjpKyPNCgoKPpKWz-aw9Jtd1uVG0aM130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
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dgn-np:NP1369146.RANoNP3dpUx5ChKyjpKyPNCgoKPpKWz-aw9Jtd1uVG0aM130_provenance {
  dgn-np:NP1369146.RANoNP3dpUx5ChKyjpKyPNCgoKPpKWz-aw9Jtd1uVG0aM130_assertion dcterms:description
      "[Our results lead us to the following conclusions: a) the altered p53 gene product is detectable employing the chosen mouse anti-human MoAB in decalcified, formalin fixed, paraffin-wax embedded, routine tissue sections of OSs and breast carcinomas which provides an opportunity for numerous retrospective studies and comparison with additional immunodiagnostic indicators; b) primary OSs with similar cell differentiation may be genetically heterogeneous; c) p53 gene or protein alterations represent early, immunodiagnostic markers of a malignant immunophenotype (IP) in various human neoplasms, including OSs; and d) immunomorphological techniques and in situ hybridization should be employed as methods to collect data for computerized, quantitative image analysis (IA) of the cellular accumulation and localization of the altered p53 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP1369146.RANoNP3dpUx5ChKyjpKyPNCgoKPpKWz-aw9Jtd1uVG0aM130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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