@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac> .
@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:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_head {
  this: np:hasAssertion dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_assertion;
    np:hasProvenance dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_provenance;
    np:hasPublicationInfo dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_assertion a np:Assertion .
  
  dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_provenance a np:Provenance .
  
  dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_assertion {
  miriam-gene:50964 a ncit:C16612 .
  
  lld:C0432272 a ncit:C7057 .
  
  dgn-gda:DGNee49cb2553e0eb62872c99941b987047 sio:SIO_000628 miriam-gene:50964, lld:C0432272;
    a sio:SIO_001121 .
}

dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_provenance {
  dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_assertion dcterms:description
      "[The exclusive bone phenotype of good quality of patients with sclerosteosis and Van Buchem disease and the specific localization of sclerostin make it an attractive target for the development of bone forming therapeutics.]. 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:15869900;
    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:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:40+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" .
}