@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP820752.RAaWbVHqnAzppJ1vbyQQ-_RK89fzMzBstDPUwiSdUfVSs> .
@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:NP820752.RAaWbVHqnAzppJ1vbyQQ-_RK89fzMzBstDPUwiSdUfVSs130_head {
  this: np:hasAssertion dgn-np:NP820752.RAaWbVHqnAzppJ1vbyQQ-_RK89fzMzBstDPUwiSdUfVSs130_assertion;
    np:hasProvenance dgn-np:NP820752.RAaWbVHqnAzppJ1vbyQQ-_RK89fzMzBstDPUwiSdUfVSs130_provenance;
    np:hasPublicationInfo dgn-np:NP820752.RAaWbVHqnAzppJ1vbyQQ-_RK89fzMzBstDPUwiSdUfVSs130_publicationInfo;
    a np:Nanopublication .
  
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dgn-np:NP820752.RAaWbVHqnAzppJ1vbyQQ-_RK89fzMzBstDPUwiSdUfVSs130_assertion {
  miriam-gene:3429 a ncit:C16612 .
  
  lld:C0035335 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP820752.RAaWbVHqnAzppJ1vbyQQ-_RK89fzMzBstDPUwiSdUfVSs130_provenance {
  dgn-np:NP820752.RAaWbVHqnAzppJ1vbyQQ-_RK89fzMzBstDPUwiSdUfVSs130_assertion dcterms:description
      "[In this chapter, we compare the phenotypes of the different conventional Men1 knockouts, detail the similarities and differences between Men1 pathogenesis in mice and humans and highlight results from recent crossbreeding studies between Men1 mutants and mice with null mutations in genes within the retinoblastoma pathway, including p18(Inc4c), p27(Kip1) and Rb.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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  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:NP820752.RAaWbVHqnAzppJ1vbyQQ-_RK89fzMzBstDPUwiSdUfVSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:22+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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    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>,
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