@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk> .
@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:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_head {
  this: np:hasAssertion dgn-np:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_assertion;
    np:hasProvenance dgn-np:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_provenance;
    np:hasPublicationInfo dgn-np:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_assertion a np:Assertion .
  
  dgn-np:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_provenance a np:Provenance .
  
  dgn-np:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_assertion {
  miriam-gene:25870 a ncit:C16612 .
  
  lld:C0266273 a ncit:C7057 .
  
  dgn-gda:DGN1c3e975802134d4ba9c668a4b8f8f7fa sio:SIO_000628 miriam-gene:25870, lld:C0266273;
    a sio:SIO_001121 .
}

dgn-np:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_provenance {
  dgn-np:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_assertion dcterms:description
      "[These results demonstrate the applicability of PFGE for analysis of Xp21, and should facilitate the mapping of other translocations and deletions in this region, some of which lead to glycerol kinase deficiency and adrenal hypoplasia as well as 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:3026644;
    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:NP699803.RAWTLMKSaiNKzkWCWPxcmPdtVh4GdWNnoMjbGYhAZ2EOk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:05+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" .
}