@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc> .
@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:NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc130_head {
  this: np:hasAssertion dgn-np:NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc130_assertion ;
    np:hasProvenance dgn-np:NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc130_provenance ;
    np:hasPublicationInfo dgn-np:NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc130_provenance a np:Provenance .
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}
dgn-np:NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc130_assertion {
  miriam-gene:8074 a ncit:C16612 .
  lld:C0342643 a ncit:C7057 .
  dgn-gda:DGN9a46f63b945743983987c255e862e999 sio:SIO_000628 miriam-gene:8074 , lld:C0342643 ;
    a sio:SIO_001121 .
}
dgn-np:NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc130_provenance {
  dgn-np:NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc130_assertion dcterms:description "[To test endogenous DMP1 response to serum metabolites that also regulate FGF23, UMR-106 cells were treated with 1,25(OH)(2) vitamin D (1x10(-7) M) and showed a 12-fold increase in DMP1 mRNA and protein at 24 h. In summary, we have identified a novel DMP1 deletion as the cause of ARHR, as well as demonstrated that the ARHR mutations alter DMP1 cellular processing, and that DMP1 can be regulated by vitamin D. Taken together, this work expands our understanding of the genetic and molecular mechanisms associated with DMP1 alterations causing ARHR.]. 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:19007919 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP377709.RA5vD1RX3ucpeptlaRIIP23pPJNMR52rH1A5-W5_0dHDc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:41+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> ;
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