@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU> .
@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:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_head {
  this: np:hasAssertion dgn-np:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_assertion ;
    np:hasProvenance dgn-np:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_provenance ;
    np:hasPublicationInfo dgn-np:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_assertion a np:Assertion .
  dgn-np:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_provenance a np:Provenance .
  dgn-np:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_assertion {
  miriam-gene:673 a ncit:C16612 .
  lld:C0007115 a ncit:C7057 .
  dgn-gda:DGNb89b8459617be270fd589f1a67705480 sio:SIO_000628 miriam-gene:673 , lld:C0007115 ;
    a sio:SIO_001122 .
}
dgn-np:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_provenance {
  dgn-np:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_assertion dcterms:description "[These data clearly confirm that BRAF(V599E) is the more common genetic alteration found to date in adult sporadic PTCs, that it is unique for this thyroid cancer histotype, and that it might drive the development of PTCs of the classic papillary subtype.]. 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:15126572 ;
    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:NP442867.RAx2sUL475_T0IwaldhAZXGl2WzglIM89kZ_VkeC1-BNU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:06+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" .
}