@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c> .
@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:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_head {
  this: np:hasAssertion dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_assertion;
    np:hasProvenance dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_provenance;
    np:hasPublicationInfo dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_assertion a np:Assertion .
  
  dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_provenance a np:Provenance .
  
  dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_assertion {
  miriam-gene:4221 a ncit:C16612 .
  
  lld:C0021670 a ncit:C7057 .
  
  dgn-gda:DGNdb8b764ecc391b50bef0392b0d960846 sio:SIO_000628 miriam-gene:4221, lld:C0021670;
    a sio:SIO_001121 .
}

dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_provenance {
  dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_assertion dcterms:description
      "[The lower rate of 11q13 LOH in MEN1-associated and sporadic gastrinomas and sporadic insulinomas as compared to MEN1 nongastrinomas may reflect alternative genetic pathways for the development of these tumors or mechanisms of the MEN1 gene inactivation that do not involve large deletions.]. 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:9187127;
    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:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:27+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" .
}