@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o> .
@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:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_head {
  this: np:hasAssertion dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_assertion;
    np:hasProvenance dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_provenance;
    np:hasPublicationInfo dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_assertion a np:Assertion .
  
  dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_provenance a np:Provenance .
  
  dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_assertion {
  miriam-gene:199699 a ncit:C16612 .
  
  lld:C2678504 a ncit:C7057 .
  
  dgn-gda:DGN617de338871dbe1f594c7d654f7dccbd sio:SIO_000628 miriam-gene:199699, lld:C2678504;
    a sio:SIO_001121 .
}

dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_provenance {
  dgn-np:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_assertion dcterms:description
      "[While the mechanisms that underlie this association remain to be defined, the COLIA1 Sp1 polymorphism appears to be an important marker for low bone mass and vertebral fracture, raising the possibility that genotyping at this site may be of value in identifying women who are at risk of osteoporosis.]. 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:8841196;
    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:NP526986.RA4wcJyNh0NCkzwVMvpxn4p7HaSOzBGqO0LdvobSNOl2o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:16+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" .
}