@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE> .
@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:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_head {
  this: np:hasAssertion dgn-np:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_assertion ;
    np:hasProvenance dgn-np:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_provenance ;
    np:hasPublicationInfo dgn-np:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_assertion a np:Assertion .
  dgn-np:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_provenance a np:Provenance .
  dgn-np:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_assertion {
  miriam-gene:5592 a ncit:C16612 .
  lld:C0026986 a ncit:C7057 .
  dgn-gda:DGNa6cfb5740dbe0e0c5424a146abbd4c4e sio:SIO_000628 miriam-gene:5592 , lld:C0026986 ;
    a sio:SIO_001121 .
}
dgn-np:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_provenance {
  dgn-np:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_assertion dcterms:description "[Amplifying a polymorphic portion of the X chromosome-linked phosphoglycerate kinase (PGK) gene after selective digestion of the active X chromosome with a methylation-sensitive restriction enzyme gave results fully concordant with standard Southern blotting of DNA samples from normal (polyclonal) polymorphonuclear cells (PMN) as well as clonal PMN from patients with myelodysplastic syndrome and polycythemia vera (PCV).]. 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:1862109 ;
    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:NP717927.RAD2l4MYzr9hnshQQTxt2wm-8eY-sRBIRXW-6N8y-njvE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:16+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" .
}