@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo> .
@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:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_head {
  this: np:hasAssertion dgn-np:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_assertion ;
    np:hasProvenance dgn-np:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_provenance ;
    np:hasPublicationInfo dgn-np:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_assertion a np:Assertion .
  dgn-np:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_provenance a np:Provenance .
  dgn-np:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  lld:C1266044 a ncit:C7057 .
  dgn-gda:DGNa3d997ac66c4542677c9f97a2edd8c27 sio:SIO_000628 miriam-gene:7421 , lld:C1266044 ;
    a sio:SIO_001121 .
}
dgn-np:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_provenance {
  dgn-np:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_assertion dcterms:description "[The preferential expression of VDR in chromophobe RCCs, oncocytomas, and collecting duct carcinomas is in agreement with the concept that these tumors differentiate toward epithelium lining the distal convoluted tubules and collecting ducts.]. 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:16949927 ;
    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:NP376374.RAKHjkSYQ0jZCNPtHNtIsEEVHgJfPKT4Lb53gd8V_EQVo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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" .
}