@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo> .
@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:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_head {
  this: np:hasAssertion dgn-np:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_assertion;
    np:hasProvenance dgn-np:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_provenance;
    np:hasPublicationInfo dgn-np:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_assertion a np:Assertion .
  
  dgn-np:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_provenance a np:Provenance .
  
  dgn-np:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_assertion {
  miriam-gene:4221 a ncit:C16612 .
  
  lld:C0014132 a ncit:C7057 .
  
  dgn-gda:DGN44590665ee9449a62b9d3018ad7614a6 sio:SIO_000628 miriam-gene:4221, lld:C0014132;
    a sio:SIO_001121 .
}

dgn-np:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_provenance {
  dgn-np:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_assertion dcterms:description
      "[Familial isolated pituitary tumor and atypical familial MEN1 consisting of only pituitary tumor and hyperparathyroidism usually lack germline MEN1 mutations, suggesting that these familial endocrine tumor syndromes are genetic entities distinct from MEN1.]. 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:11740047;
    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:NP338622.RAiet0wVNWSd2IUVFle24ehTx-0bO90r8xpvW-n94Uhvo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:19+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" .
}