@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs> .
@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/v3.0.0/void/> .

dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_head {
  this: np:hasAssertion dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_assertion;
    np:hasProvenance dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_provenance;
    np:hasPublicationInfo dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_assertion a np:Assertion .
  
  dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_provenance a np:Provenance .
  
  dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_assertion {
  miriam-gene:1616 a ncit:C16612 .
  
  lld:C1845055 a ncit:C7057 .
  
  dgn-gda:DGN8b713b1525f671bad01d6e4d8ef2e084 sio:SIO_000628 miriam-gene:1616, lld:C1845055;
    a sio:SIO_001121 .
}

dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_provenance {
  dgn-np:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_assertion dcterms:description
      "[In particular, mutations of the telomere binding proteins alpha thalassemia/mental retardation syndrome X-linked (ATRX) or death-domain associated protein (DAXX) have been shown to underlie a telomere maintenance mechanism not involving telomerase (alternative lengthening of telomeres), and point mutations in the promoter of the telomerase reverse transcriptase (TERT) gene increase telomerase expression and have been shown to occur in melanomas and a small number of other tumors.]. 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:23530248;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP347492.RAlofoKfjMY4zpc4xfjYt4VGWjzOwgMQe0QY7ljKvEObs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:00+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}