@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY> .
@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:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_head {
  this: np:hasAssertion dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_assertion;
    np:hasProvenance dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_provenance;
    np:hasPublicationInfo dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_assertion a np:Assertion .
  
  dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_provenance a np:Provenance .
  
  dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_assertion {
  miriam-gene:1027 a ncit:C16612 .
  
  lld:C0027662 a ncit:C7057 .
  
  dgn-gda:DGNdc83bd262570b540682174de9add10f1 sio:SIO_000628 miriam-gene:1027, lld:C0027662;
    a sio:SIO_001121 .
}

dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_provenance {
  dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_assertion dcterms:description
      "[have reported that germline mutations in CDKN1B can predispose to the development of multiple endocrine tumours in both rats and humans and this new MEN syndrome is named MENX and MEN4, respectively.]. 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:23140918;
    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:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:34+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" .
}