@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8> .
@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:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_head {
  this: np:hasAssertion dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_assertion ;
    np:hasProvenance dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_provenance ;
    np:hasPublicationInfo dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_assertion a np:Assertion .
  dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_provenance a np:Provenance .
  dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_assertion {
  miriam-gene:51172 a ncit:C16612 .
  lld:C0038506 a ncit:C7057 .
  dgn-gda:DGNf06a390911082c4fcda104c94654540f sio:SIO_000628 miriam-gene:51172 , lld:C0038506 ;
    a sio:SIO_001121 .
}
dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_provenance {
  dgn-np:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_assertion dcterms:description "[While data on the GlcNAc-phosphotransferase encoded by GNPTAB/G remains limited and only suggestive, a study of the enzyme encoded by NAGPA has shown that the mutations found in stuttering reduce the overall cellular activity of this enzyme by about half, and that they result in deficits in intracellular processing and trafficking that lead to a reduced cellular half life.]. 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:22884963 ;
    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:NP587772.RARq4JJ20y8lpAMQetCl2HZ-3tVTEr4QJYIs2SQtSW3C8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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" .
}