@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y> .
@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:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_head {
  this: np:hasAssertion dgn-np:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_assertion;
    np:hasProvenance dgn-np:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_provenance;
    np:hasPublicationInfo dgn-np:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_assertion a np:Assertion .
  
  dgn-np:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_provenance a np:Provenance .
  
  dgn-np:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_assertion {
  miriam-gene:79577 a ncit:C16612 .
  
  lld:C0687150 a ncit:C7057 .
  
  dgn-gda:DGN9676d4c01c7cc51065f8e0e88122564e sio:SIO_000628 miriam-gene:79577, lld:C0687150;
    a sio:SIO_001121 .
}

dgn-np:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_provenance {
  dgn-np:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_assertion dcterms:description
      "[In light of the strong association between mutations of HRPT2 and sporadic parathyroid carcinoma demonstrated in this study, it is hypothesised that HRPT2 mutation is an early event that may lead to parathyroid malignancy and suggest intragenic mutation of HRPT2 as a marker of malignant potential in both familial and sporadic parathyroid tumours.]. 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:12960210;
    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:NP407955.RARaflk__e18pErwCnH-fKXiAlLG99P3WyHpVkeiAhY3Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:50+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" .
}