@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_head {
  this: np:hasAssertion dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_assertion;
    np:hasProvenance dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_provenance;
    np:hasPublicationInfo dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_assertion a np:Assertion .
  
  dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_provenance a np:Provenance .
  
  dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0029456 a ncit:C7057 .
  
  dgn-gda:DGN970f7232317ba0b08e40e7146a59c7f9 sio:SIO_000628 miriam-gene:1756, lld:C0029456;
    a sio:SIO_001121 .
}

dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_provenance {
  dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_assertion dcterms:description
      "[Mutations in the LRP5 gene on chromosome 11q12-13 have been associated with rare syndromes characterized by extremely low or high BMD, but little is known about the contribution of this gene to the development of osteoporosis and determination of BMD in a normal population.]. 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:15355556;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:13+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}