@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_head {
  this: np:hasAssertion dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_assertion ;
    np:hasProvenance dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_provenance ;
    np:hasPublicationInfo dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_assertion a np:Assertion .
  dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_provenance a np:Provenance .
  dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_assertion {
  miriam-gene:2710 a ncit:C16612 .
  lld:C0220766 a ncit:C7057 .
  dgn-gda:DGNa29bb51c1ed0a31a961711dcd0b14b43 sio:SIO_000628 miriam-gene:2710 , lld:C0220766 ;
    a sio:SIO_001121 .
}
dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_provenance {
  dgn-np:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_assertion dcterms:description "[Complex glycerol kinase deficiency (GKD) results from the contiguous deletion on Xp21 of all or part of the gene for glycerol kinase together with that for adrenal hypoplasia congenita (AHC) and /or Duchenne muscular dystrophy (DMD).]. 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:15684452 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP426720.RAgjmBbSkj2ekjDcMs-ClWrvJR2_8NYW-QcGa-bRBY6Vc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:48+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}