@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8> .
@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:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_head {
  this: np:hasAssertion dgn-np:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_assertion ;
    np:hasProvenance dgn-np:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_provenance ;
    np:hasPublicationInfo dgn-np:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_assertion a np:Assertion .
  dgn-np:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_provenance a np:Provenance .
  dgn-np:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_assertion {
  miriam-gene:1508 a ncit:C16612 .
  lld:C0410528 a ncit:C7057 .
  dgn-gda:DGN6b42602ec7558d8fb783d78ab6bcbf6f sio:SIO_000628 miriam-gene:1508 , lld:C0410528 ;
    a sio:SIO_001121 .
}
dgn-np:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_provenance {
  dgn-np:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_assertion dcterms:description "[Pycnodysostosis (Pycno) is an autosomal recessive osteosclerotic skeletal dysplasia that is caused by the markedly deficient activity of cathepsin K. This lysosomal cysteine protease has substantial collagenase activity, is present at high levels in osteoclasts, and is secreted into the subosteoclastic space where bone matrix is degraded.]. 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:10571690 ;
    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:NP906994.RAE6R_8_WS5bpMzLlFnrI0u5QEX9RkQ_9qWcOdHPMTlp8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:17+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" .
}