@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI> .
@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:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_head {
  this: np:hasAssertion dgn-np:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_assertion;
    np:hasProvenance dgn-np:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_provenance;
    np:hasPublicationInfo dgn-np:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_assertion a np:Assertion .
  
  dgn-np:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_provenance a np:Provenance .
  
  dgn-np:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_assertion {
  miriam-gene:10518 a ncit:C16612 .
  
  lld:C0020459 a ncit:C7057 .
  
  dgn-gda:DGNc5a693f8f4a6855eedb59f2b2573c62e sio:SIO_000628 miriam-gene:10518, lld:C0020459;
    a sio:SIO_001121 .
}

dgn-np:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_provenance {
  dgn-np:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_assertion dcterms:description
      "[In order to evaluate whether all cases of focal hyperinsulinism are caused by this mechanism, 56 pancreatectomy specimens with focal hyperinsulinism were tested for the loss of maternal allele by two methods: immunohistochemistry for p57(kip2) (n=56) and microsatellite marker analysis (n=27).]. 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:16357843;
    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:NP350304.RAhyuuFdl5E-GJ_NWRTq8ZeKDHxYRNeLoK3EGwaowy8cI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:25+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" .
}