@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_head {
   this: np:hasAssertion dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_assertion ;
    np:hasProvenance dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_provenance ;
    np:hasPublicationInfo dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_assertion a np:Assertion .
  dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_provenance a np:Provenance .
  dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_assertion {
   miriam-gene:5741 a ncit:C16612 .
  lld:C3536984 a ncit:C7057 .
  dgn-gda:DGN092c4e46a932c407db696fc579ac361c sio:SIO_000628 miriam-gene:5741 , lld:C3536984 ;
    a sio:SIO_001121 .
}
dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_provenance {
   dgn-np:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_assertion dcterms:description "[Oncogenic osteomalacia (OOM), X-linked hypophosphatemia (XLH), and autosomal dominant hypophosphatemic rickets (ADHR) are phenotypically similar disorders characterized by hypophosphatemia, decreased renal phosphate reabsorption, normal or low serum calcitriol concentrations, normal serum concentrations of calcium and parathyroid hormone, and defective skeletal mineralization.]. 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:11409890 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP321164.RA43wXq27yAj8yTHmwmPbvTX1n0lNmRQbrJqqrzc4YGGs130_publicationInfo {
   this: dcterms:created "2016-05-13T12:44:11+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}