@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I> .
@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:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_head {
  this: np:hasAssertion dgn-np:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_assertion;
    np:hasProvenance dgn-np:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_provenance;
    np:hasPublicationInfo dgn-np:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_assertion a np:Assertion .
  
  dgn-np:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_provenance a np:Provenance .
  
  dgn-np:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_assertion {
  miriam-gene:4221 a ncit:C16612 .
  
  lld:C0030521 a ncit:C7057 .
  
  dgn-gda:DGN83ed504d85567cf477cb3515df1af6b5 sio:SIO_000628 miriam-gene:4221, lld:C0030521;
    a sio:SIO_001121 .
}

dgn-np:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_provenance {
  dgn-np:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_assertion dcterms:description
      "[Germ-line mutations of the MEN1 gene, located at 11q13, have been demonstrated in MEN1 kindreds, and loss of heterozygosity (LOH) on 11q13 together with somatic MEN1 mutations have been detected in 20% of nonfamilial parathyroid tumors.]. 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:9458074;
    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:NP204236.RAj4sUPO6IWxkqTBxclub8ke-rBzm6pp1dt8O00Ci9V6I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:52+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" .
}