@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I> .
@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:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_head {
  this: np:hasAssertion dgn-np:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_assertion;
    np:hasProvenance dgn-np:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_provenance;
    np:hasPublicationInfo dgn-np:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_assertion a np:Assertion .
  
  dgn-np:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_provenance a np:Provenance .
  
  dgn-np:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_assertion {
  miriam-gene:450095 a ncit:C16612 .
  
  lld:C0876973 a ncit:C7057 .
  
  dgn-gda:DGNd1de6f566f5b47bb18ed11b730ce03f4 sio:SIO_000628 miriam-gene:450095, lld:C0876973;
    a sio:SIO_001121 .
}

dgn-np:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_provenance {
  dgn-np:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_assertion dcterms:description
      "[Systematic screening with an oral glucose tolerance test is recommended from the age of 14 years because clinical signs of CFRD are often confused with signs of pulmonary infection and CFRD occurrence is associated with weight and pulmonary function deterioration.]. 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:16142013;
    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:NP716724.RAISTWoWFLFhHpE2aEohpCvzEGL7duk75de4ntHYgdb1I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:15+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" .
}