@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY> .
@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:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_head {
  this: np:hasAssertion dgn-np:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_assertion;
    np:hasProvenance dgn-np:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_provenance;
    np:hasPublicationInfo dgn-np:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_assertion a np:Assertion .
  
  dgn-np:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_provenance a np:Provenance .
  
  dgn-np:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  
  lld:C0035579 a ncit:C7057 .
  
  dgn-gda:DGNee1d529b078a214b9e0a6dfb126d3fe6 sio:SIO_000628 miriam-gene:7421, lld:C0035579;
    a sio:SIO_001122 .
}

dgn-np:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_provenance {
  dgn-np:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_assertion dcterms:description
      "[Postulating that vitamin D receptor (VDR) polymorphisms might relate to the susceptibility of some Nigerian children to develop rickets in the setting of low calcium intake, we compared the VDR genotypes, as determined by the presence or absence of Bsm I, Apa I, Taq I, and Fok I restriction enzyme cleavage sites, between 105 children with active nutritional rickets and 94 subjects representative of the community from which the rachitic children came.]. 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:11092401;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP59089.RAbOw7JWtfcSPkupmJknd8tpS3ZegNziriDU9URwf2_aY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}