@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro> .
@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 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:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_head {
  this: np:hasAssertion dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_assertion ;
    np:hasProvenance dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_provenance ;
    np:hasPublicationInfo dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_assertion a np:Assertion .
  dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_provenance a np:Provenance .
  dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_assertion {
  miriam-gene:1557 a ncit:C16612 .
  lld:C0038354 a ncit:C7057 .
  dgn-gda:DGNdc35a94de21e849f921ff9e83238d6e4 sio:SIO_000628 miriam-gene:1557 , lld:C0038354 ;
    a sio:SIO_001122 .
}
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_provenance {
  dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_assertion dct:description "[ The combination regimen of famotidine plus rabeprazole is more effective for nocturnal acid inhibition in homozygous and heterozygous EMs than the increased dosage regimen of rabeprazole. This concomitant therapy could be a rescue regimen for patients with nocturnal acid breakthrough refractory to a standard PPI therapy who are likely to be CYP2C19 EMs.]. 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:15903128 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}