@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0> .
@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:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_head {
  this: np:hasAssertion dgn-np:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_assertion;
    np:hasProvenance dgn-np:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_provenance;
    np:hasPublicationInfo dgn-np:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_assertion a np:Assertion .
  
  dgn-np:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_provenance a np:Provenance .
  
  dgn-np:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_assertion {
  miriam-gene:1027 a ncit:C16612 .
  
  lld:C0027662 a ncit:C7057 .
  
  dgn-gda:DGN88046e51a1deb9632f117f6ab6df4efb sio:SIO_000628 miriam-gene:1027, lld:C0027662;
    a sio:SIO_001121 .
}

dgn-np:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_provenance {
  dgn-np:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_assertion dcterms:description
      "[Recently, germline mutations in CDKN1B have been associated with the inherited multiple endocrine neoplasia syndrome type 4, an autosomal dominant syndrome characterized by varying combinations of tumors affecting at least two endocrine organs.]. 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:23555276;
    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:NP294913.RAvxPJYE9X6cmhpHZ3pjOkqO2g-mg5bRLNm7gdb2UdYs0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:47+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" .
}