@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI> .
@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:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_head {
  this: np:hasAssertion dgn-np:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_assertion;
    np:hasProvenance dgn-np:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_provenance;
    np:hasPublicationInfo dgn-np:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_assertion a np:Assertion .
  
  dgn-np:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_provenance a np:Provenance .
  
  dgn-np:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_assertion {
  miriam-gene:796 a ncit:C16612 .
  
  lld:C0238463 a ncit:C7057 .
  
  dgn-gda:DGN9270773eea38d9755bf080d277a050f7 sio:SIO_000628 miriam-gene:796, lld:C0238463;
    a sio:SIO_001121 .
}

dgn-np:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_provenance {
  dgn-np:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_assertion dcterms:description
      "[In addition to an analysis of rearranged during transfection mutations and calcitonin profiles in medullary thyroid carcinoma, this review includes emphasis on familial nonmedullary thyroid cancer syndromes, including genetic findings in familial papillary thyroid cancer, familial adenomatous polyposis, Cowden syndrome, Carney complex, and Werner syndrome.]. 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:20729730;
    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:NP647446.RArQnC9VxXPLwynqEZpEAmschL3OUOcppw8bO-PY_X6YI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:30+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" .
}