@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs> .
@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:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_head {
   this: np:hasAssertion dgn-np:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_assertion ;
    np:hasProvenance dgn-np:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_provenance ;
    np:hasPublicationInfo dgn-np:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_assertion a np:Assertion .
  dgn-np:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_provenance a np:Provenance .
  dgn-np:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_assertion {
   miriam-gene:8074 a ncit:C16612 .
  lld:C0029442 a ncit:C7057 .
  dgn-gda:DGN22cfa4440d89126789dd2c20419b6c16 sio:SIO_000628 miriam-gene:8074 , lld:C0029442 ;
    a sio:SIO_001121 .
}
dgn-np:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_provenance {
   dgn-np:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_assertion dcterms:description "[Pathologically, high circulating levels of FGF23 result in hypophosphatemia, decreased production of 1,25(OH)(2)D, elevated parathyroid hormone and rickets/osteomalacia in patients with functioning kidneys, whereas low levels are associated with tumoral calcinosis, hyperphosphatemia and elevated 1,25(OH)(2)D. In addition, patients with chronic kidney disease (CKD) exhibit marked elevations of circulating FGF23.]. 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:17635819 ;
    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:NP172798.RALd65h3SAJKLsmSh271zgVcCmbc8U48DmEgxzYb27rrs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:33+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" .
}