@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk> .
@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:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_head {
  this: np:hasAssertion dgn-np:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_assertion ;
    np:hasProvenance dgn-np:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_provenance ;
    np:hasPublicationInfo dgn-np:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_assertion a np:Assertion .
  dgn-np:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_provenance a np:Provenance .
  dgn-np:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_assertion {
  miriam-gene:5251 a ncit:C16612 .
  lld:C0342653 a ncit:C7057 .
  dgn-gda:DGNcd2db68d7e350abe1180136fd52a9c6e sio:SIO_000628 miriam-gene:5251 , lld:C0342653 ;
    a sio:SIO_001121 .
}
dgn-np:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_provenance {
  dgn-np:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_assertion dcterms:description "[Recent studies of inherited and acquired hypophosphatemia which exhibit similar biochemical and clinical features, have led to the identification of novel genes, phosphate regulating gene with homologies to endopeptidases on the X chromosome (PHEX) and fibroblast growth factor-23 (FGF-23), that play a role in the regulation of Pi homeostasis.]. 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:15630224 ;
    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:NP279459.RAxCiDVKj6TpvdZIbM9MkdwtSbBPOb30B5VgvzBBwkTVk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:37+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" .
}