@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho> .
@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/v3.0.0/void/> .
dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_head {
  this: np:hasAssertion dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_assertion ;
    np:hasProvenance dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_provenance ;
    np:hasPublicationInfo dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_assertion a np:Assertion .
  dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_provenance a np:Provenance .
  dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_assertion {
  miriam-gene:79651 a ncit:C16612 .
  lld:C0546837 a ncit:C7057 .
  dgn-gda:DGN9a2c16a208e3ae673f56ed23c6065d4b sio:SIO_000628 miriam-gene:79651 , lld:C0546837 ;
    a sio:SIO_001121 .
}
dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_provenance {
  dgn-np:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_assertion dcterms:description "[Earlier loss of heterozygosity (or allelic imbalance) studies have implicated regions on chromosomes 3p, 5q, 9p, 13q, 17p, 17q, and 18q in the development of sporadic oesophageal cancer and recent data have linked the familial tylosis with oesophageal cancer (TOC) gene-containing region on chromosome 17q25 with this cancer.]. 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:15254736 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP944858.RAt5zYqR3wTBDeutKEVtF-RqPAN_O6IHBEMC_WF7tNwho130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:17+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}