@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI> .
@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:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_head {
  this: np:hasAssertion dgn-np:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_assertion;
    np:hasProvenance dgn-np:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_provenance;
    np:hasPublicationInfo dgn-np:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_assertion a np:Assertion .
  
  dgn-np:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_provenance a np:Provenance .
  
  dgn-np:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0272170 a ncit:C7057 .
  
  dgn-gda:DGN1665de6a2583a4035a07f5d996ee8918 sio:SIO_000628 miriam-gene:1756, lld:C0272170;
    a sio:SIO_001121 .
}

dgn-np:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_provenance {
  dgn-np:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_assertion dcterms:description
      "[Eleven patients (8 males) aged from 5 to 37 years (median 16.7 years) with a genetically confirmed diagnosis of SDS were assessed for fracture history, bone mineral content (BMC), lean tissue mass (LTM) and bone mineral density (BMD) (Hologic Discovery A), osteoporotic vertebral changes, and for blood biochemistry and hematological parameters.]. 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:17920346;
    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:NP249138.RADY9876szP1JzBnSV_RlDOthHozy7DImgfGteAzlXPGI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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" .
}