@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw> .
@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:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_head {
  this: np:hasAssertion dgn-np:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_assertion ;
    np:hasProvenance dgn-np:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_provenance ;
    np:hasPublicationInfo dgn-np:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_assertion a np:Assertion .
  dgn-np:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_provenance a np:Provenance .
  dgn-np:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_assertion {
  miriam-gene:7012 a ncit:C16612 .
  lld:C1623038 a ncit:C7057 .
  dgn-gda:DGN3627ad51215454e6fcdba916abb4a469 sio:SIO_000628 miriam-gene:7012 , lld:C1623038 ;
    a sio:SIO_001121 .
}
dgn-np:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_provenance {
  dgn-np:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_assertion dcterms:description "[In all, 134 patients with cirrhosis of common etiologies treated at the Liver Research Institute, University of Arizona, between May 2008 and July 2009, and 528 healthy subjects were screened for variation in the TERT and TERC genes by direct sequencing; an additional 1,472 controls were examined for the most common genetic variation observed in patients.]. 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:21520173 ;
    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:NP921201.RAg4H1sRmcsc8GtIvSh2-uY60J84Kv6YDQIyxVxK8tIRw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:25+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" .
}