@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ> .
@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:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_head {
  this: np:hasAssertion dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_assertion ;
    np:hasProvenance dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_assertion a np:Assertion .
  dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_provenance a np:Provenance .
  dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_assertion {
  miriam-gene:7015 a ncit:C16612 .
  lld:C2239176 a ncit:C7057 .
  dgn-gda:DGNb49acb79496f7fab891c80f6568a0120 sio:SIO_000628 miriam-gene:7015 , lld:C2239176 ;
    a sio:SIO_001121 .
}
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_provenance {
  dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_assertion dcterms:description "[Due to the systemic involvement of telomerase diseases very likely influencing the clinical outcome, and the peculiar biological features of hepatocellular carcinoma arising in this context, we suggest that patients with cryptogenic cirrhosis or other suggestive features should be screened for TERT mutations and specific treatment algorithms elaborated for this disease.]. 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:23000435 ;
    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:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:34+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" .
}