@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM> .
@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:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_head {
  this: np:hasAssertion dgn-np:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_assertion;
    np:hasProvenance dgn-np:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_provenance;
    np:hasPublicationInfo dgn-np:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_assertion a np:Assertion .
  
  dgn-np:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_provenance a np:Provenance .
  
  dgn-np:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_assertion {
  miriam-gene:5741 a ncit:C16612 .
  
  lld:C0020437 a ncit:C7057 .
  
  dgn-gda:DGNee347cf3092c41f01c66b75a76bcc99c sio:SIO_000628 miriam-gene:5741, lld:C0020437;
    a sio:SIO_001121 .
}

dgn-np:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_provenance {
  dgn-np:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_assertion dcterms:description
      "[The same mutation pattern was seen in both the proband's younger brother and cousin diagnosed as MEN1, and was also observed in the son of the cousin who showed signs of normal levels of serum PTH associated with mild hypercalcemia and hypophosphatemia.]. 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:10395246;
    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:NP256732.RAvZiJdCddRJAUerv0vtFstnxTrVZ0nBfdGjxNIufhEmM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:42+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" .
}