@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc> .
@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:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_head {
  this: np:hasAssertion dgn-np:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_assertion ;
    np:hasProvenance dgn-np:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_provenance ;
    np:hasPublicationInfo dgn-np:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_assertion a np:Assertion .
  dgn-np:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_provenance a np:Provenance .
  dgn-np:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_assertion {
  miriam-gene:8030 a ncit:C16612 .
  lld:C1458156 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_provenance {
  dgn-np:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_assertion dcterms:description "[Although we found accumulation of mutations in two older patients with PTC and one patient with FTC (all three patients older than 45 years had mtDNA mutations), the low frequency of these mutations in the small group of 10 analyzed patients did not correlate with statistically validated clinical prognosticators for recurrence or survival, especially not with age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP213486.RAgGV-k3POGxPZFxuD10vxhdoXmjncRXohqPguSrfAfXc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}