@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc> .
@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:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_head {
  this: np:hasAssertion dgn-np:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_assertion;
    np:hasProvenance dgn-np:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_provenance;
    np:hasPublicationInfo dgn-np:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_assertion a np:Assertion .
  
  dgn-np:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_provenance a np:Provenance .
  
  dgn-np:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_assertion {
  miriam-gene:5111 a ncit:C16612 .
  
  lld:C0546837 a ncit:C7057 .
  
  dgn-gda:DGN7e7ad356a8800b5ed8b1697dc14b3a96 sio:SIO_000628 miriam-gene:5111, lld:C0546837;
    a sio:SIO_001121 .
}

dgn-np:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_provenance {
  dgn-np:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_assertion dcterms:description
      "[The most common alterations found in esophageal cancers include allelic losses at chromosomes 3p, 5q, 9p, 9q, 13q, 17p, 17q and 18q, as well as mutations of p53 (mostly missense), Rb (deletions), cyclin DI (amplifications) and c-myc (amplifications).]. 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:8682592;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1352677.RASP2QcN28xartXEBNx1nd7rA6T78ezsF-UH81v5DSedc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:59+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}