@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM> .
@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:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_head {
  this: np:hasAssertion dgn-np:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_assertion;
    np:hasProvenance dgn-np:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_provenance;
    np:hasPublicationInfo dgn-np:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_assertion a np:Assertion .
  
  dgn-np:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_provenance a np:Provenance .
  
  dgn-np:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_assertion {
  miriam-gene:4221 a ncit:C16612 .
  
  lld:C0017150 a ncit:C7057 .
  
  dgn-gda:DGN5c93a79b318c68e1429a5e3fae89a716 sio:SIO_000628 miriam-gene:4221, lld:C0017150;
    a sio:SIO_001121 .
}

dgn-np:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_provenance {
  dgn-np:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_assertion dcterms:description
      "[This study demonstrates that alterations in the MEN1 gene are involved in about half of all sporadic gastrinomas, although no correlation between the presence of mutations and location and clinical phenotype or severity of disease has been found.]. 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:15944766;
    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:NP271121.RADxQjX6l3v4ITFTb6Noxph-Jh-a3D9oi7t4H8Qmp6eHM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:31+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" .
}