@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8> .
@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:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_head {
  this: np:hasAssertion dgn-np:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_assertion ;
    np:hasProvenance dgn-np:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_provenance ;
    np:hasPublicationInfo dgn-np:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_assertion a np:Assertion .
  dgn-np:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_provenance a np:Provenance .
  dgn-np:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
  dgn-gda:DGN11d1a2cab38a26b9f582f2eaf99f7c4a sio:SIO_000628 miriam-gene:7421 , lld:C0006142 ;
    a sio:SIO_001121 .
}
dgn-np:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_provenance {
  dgn-np:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_assertion dcterms:description "[Alterations in vitamin D-1,25 (OH)2D3 levels and polymorphisms of VDR gene have been shown to be associated with several malignant or autoimmune diseases such as sclerosis multiplex, breast cancer, diabetes mellitus, malignant melanoma, and psoriasis vulgaris.]. 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:19818218 ;
    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:NP212652.RA01dQCEOileASOQxoc-A9Q0gn_mFI_XWVDuT60Ezioj8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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" .
}