@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ> .
@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:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_head {
  this: np:hasAssertion dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_assertion;
    np:hasProvenance dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_provenance;
    np:hasPublicationInfo dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_assertion a np:Assertion .
  
  dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_provenance a np:Provenance .
  
  dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_assertion {
  miriam-gene:2778 a ncit:C16612 .
  
  lld:C0745106 a ncit:C7057 .
  
  dgn-gda:DGN633b62e20c07fd7da56613c43e4c23bf sio:SIO_000628 miriam-gene:2778, lld:C0745106;
    a sio:SIO_001121 .
}

dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_provenance {
  dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_assertion dcterms:description
      "[Osteomalacic and hyperparathyroid changes, which emanate from distinct metabolic derangements (which superimpose on the local effects of GNAS1 mutations in bone), influence, in turn, the severity and type of skeletal morbidity in FD.]. 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:12854833;
    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:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:29+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" .
}