@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4> .
@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:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_head {
  this: np:hasAssertion dgn-np:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_assertion ;
    np:hasProvenance dgn-np:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_provenance ;
    np:hasPublicationInfo dgn-np:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_assertion a np:Assertion .
  dgn-np:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_provenance a np:Provenance .
  dgn-np:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_assertion {
  miriam-gene:5251 a ncit:C16612 .
  lld:C0027709 a ncit:C7057 .
  dgn-gda:DGN8f3edf5a047755edd6be863cbceaa39d sio:SIO_000628 miriam-gene:5251 , lld:C0027709 ;
    a sio:SIO_001121 .
}
dgn-np:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_provenance {
  dgn-np:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_assertion dcterms:description "[We describe a patient with XLH caused by a novel missense mutation in the PHEX gene, who on treatment with alfacalcidol and oral phosphate had normal growth and minimal bone deformities, but who subsequently developed moderate nephrocalcinosis, significant hyperparathyroidism, hypercalcemia, renal failure, and hypertension.]. 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:18775977 ;
    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:NP883384.RAD7qBEE-U-XBZRtMqdLwh8iUtQPvHNuW7-ryMnp7PP_4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:59+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" .
}