@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0> .
@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:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_head {
  this: np:hasAssertion dgn-np:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_assertion;
    np:hasProvenance dgn-np:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_provenance;
    np:hasPublicationInfo dgn-np:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_assertion a np:Assertion .
  
  dgn-np:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_provenance a np:Provenance .
  
  dgn-np:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_assertion {
  miriam-gene:8743 a ncit:C16612 .
  
  lld:C0178874 a ncit:C7057 .
  
  dgn-gda:DGN7a7a199f4caa05c4789b4a37559dfe92 sio:SIO_000628 miriam-gene:8743, lld:C0178874;
    a sio:SIO_001121 .
}

dgn-np:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_provenance {
  dgn-np:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_assertion dcterms:description
      "[For example, a frameshift insertion/deletion (indel) is found in the coding region of TNFSF10, which disrupts the intact open reading frame and undermines the ability of TNFSF10 to induce apoptosis, in consequence promoting abnormal tumor progression.]. 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:23434521;
    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:NP1055257.RAKD3dFzYjliftVyxK8Zp5p8uk19h8HguoFe-LGH8_qD0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:44+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" .
}