@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y> .
@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/v4.0.0/void/> .

dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_head {
  this: np:hasAssertion dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_assertion;
    np:hasProvenance dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_provenance;
    np:hasPublicationInfo dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_assertion a np:Assertion .
  
  dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_provenance a np:Provenance .
  
  dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_assertion {
  miriam-gene:6736 a ncit:C16612 .
  
  lld:C0008626 a ncit:C7057 .
  
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dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_provenance {
  dgn-np:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_assertion dcterms:description
      "[The aim of the present study was to propose a feasible and practical molecular diagnostic tool for newborn screening by quantifying the gene dosage of the SHOX, VAMP7, XIST, UBA1, and SRY genes by quantitative polymerase chain reaction (qPCR) in individuals with a diagnosis of complete X monosomy, as well as those with TS variants, and then compare the results to controls without chromosomal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1250780.RAjil1vP8tYPkDnyGgmPhCM2UbuH8UkgOpQikJ7dpu32Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:13+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;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}