@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk> .
@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/v3.0.0/void/> .
dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_head {
  this: np:hasAssertion dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_assertion ;
    np:hasProvenance dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_provenance ;
    np:hasPublicationInfo dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_assertion a np:Assertion .
  dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_provenance a np:Provenance .
  dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_assertion {
  miriam-gene:4221 a ncit:C16612 .
  lld:C0025268 a ncit:C7057 .
  dgn-gda:DGNff6bb6971533f9c01f352c5db99d46f3 sio:SIO_000628 miriam-gene:4221 , lld:C0025268 ;
    a sio:SIO_001121 .
}
dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_provenance {
  dgn-np:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_assertion dcterms:description "[These data suggest that RET gene mutation may not be involved in the development of sporadic parathyroid tumors and hyperplasia secondary to uremia and that MEN1 gene mutation may not be or is rarely associated with development of parathyroid hyperplasia in MEN2A patients.]. 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:10915003 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP553275.RAIFvMAyKpqjyf5ikhz7IqLvUECVZEnwZ1y7kpdhmPyFk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:07+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}