@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE> .
@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/v4.0.0/void/> .

dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_head {
  this: np:hasAssertion dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_assertion;
    np:hasProvenance dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_provenance;
    np:hasPublicationInfo dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_assertion a np:Assertion .
  
  dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_provenance a np:Provenance .
  
  dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_assertion {
  miriam-gene:673 a ncit:C16612 .
  
  lld:C0238463 a ncit:C7057 .
  
  dgn-gda:DGN7c5e37c09c65fe734b8c9abb733fce50 sio:SIO_000628 miriam-gene:673, lld:C0238463;
    a sio:SIO_001121 .
}

dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_provenance {
  dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_assertion dcterms:description
      "[Current selection of PTC patients for CND is appropriate but higher extent of the procedure, once selected, is needed to reduce disease recurrence, which may be defined by combination use of preoperative BRAF mutation testing and conventional risk factors of PTC.]. 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:23132792;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:31+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}