@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro> .
@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:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_head {
  this: np:hasAssertion dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_assertion ;
    np:hasProvenance dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_provenance ;
    np:hasPublicationInfo dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_assertion a np:Assertion .
  dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_provenance a np:Provenance .
  dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_assertion {
  miriam-gene:1594 a ncit:C16612 .
  lld:C0342922 a ncit:C7057 .
  dgn-gda:DGN5021c4d740297858b26ce912b124fdc7 sio:SIO_000628 miriam-gene:1594 , lld:C0342922 ;
    a sio:SIO_001121 .
}
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_provenance {
  dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_assertion dcterms:description "[Although it is not clear why a presumed better-functioning VDR variant (F allele) is associated with an increased risk of developing rickets, this study raises the possibility that VDR alleles might be important in determining an individual's susceptibility to developing rickets when faced with dietary calcium deficiency.]. 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: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:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:11+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" .
}