@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE> .
@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:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_head {
  this: np:hasAssertion dgn-np:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_assertion;
    np:hasProvenance dgn-np:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_provenance;
    np:hasPublicationInfo dgn-np:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_assertion a np:Assertion .
  
  dgn-np:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_provenance a np:Provenance .
  
  dgn-np:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_assertion {
  miriam-gene:2064 a ncit:C16612 .
  
  lld:C0152018 a ncit:C7057 .
  
  dgn-gda:DGN7f486ad8760c87ec27c89d76ecb3a662 sio:SIO_000628 miriam-gene:2064, lld:C0152018;
    a sio:SIO_001121 .
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dgn-np:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_provenance {
  dgn-np:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_assertion dcterms:description
      "[We also detected significant differences in germline allele frequency between the esophageal cohort of our study and normal control samples from the International HapMap Project for 10 genes (CSF1, KIAA1804, IL2, PMS2, IRF7, FLT3, NTRK2, MAP3K9, ERBB2 and PRKAR1A), suggesting that they might play roles in esophageal cancer susceptibility and/or development.]. 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:18241037;
    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:NP653053.RAnQSR6ZdND2U3kcEQJiHiKkkjNlvnPCINj2tQeKyI3pE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:41+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>;
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    pav:version "v4.0.0.0" .
  
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}