@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI> .
@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:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_head {
  this: np:hasAssertion dgn-np:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_assertion ;
    np:hasProvenance dgn-np:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_provenance ;
    np:hasPublicationInfo dgn-np:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_assertion a np:Assertion .
  dgn-np:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_provenance a np:Provenance .
  dgn-np:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  lld:C0020676 a ncit:C7057 .
  dgn-gda:DGN3a6eb3c547b50be2a2a62de3b4345a63 sio:SIO_000628 miriam-gene:2688 , lld:C0020676 ;
    a sio:SIO_001121 .
}
dgn-np:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_provenance {
  dgn-np:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_assertion dcterms:description "[The delay in sexual maturation, the presence of diabetes and hypothyroidism, the parathyroid gland dysfunction, the progressive marrow expansion, the iron toxicity on osteoblasts, the iron chelators, and the deficiency of growth hormone or insulin growth factors have been identified as major causes of osteoporosis in thalassemia.]. 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:20712799 ;
    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:NP649014.RAUTIp44V_l89Boegtppp0R3WyS4BfOCg_HTdJtPgpZqI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:31+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" .
}