@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_head {
  this: np:hasAssertion dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_assertion;
    np:hasProvenance dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_provenance;
    np:hasPublicationInfo dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_assertion a np:Assertion .
  
  dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_provenance a np:Provenance .
  
  dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_assertion {
  miriam-gene:7251 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGNe80c8840deb1c4fd69695eb9a4ec9934 sio:SIO_000628 miriam-gene:7251, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_provenance {
  dgn-np:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_assertion dcterms:description
      "[Our results suggest that the truncated TSG101 transcripts are definitely detectable in various human leukemia and lymphoma cell lines, but do not support the notion that the variant transcripts may have a major functional relevance in the pathogenesis of human hematopoietic malignant disorder.]. 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:10664246;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP190146.RAdiTI1xpSeFvln3cAVfO0zbfDHhhDV-7VQIBLZz_rj3Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}