@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY> .
@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:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_head {
  this: np:hasAssertion dgn-np:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_assertion;
    np:hasProvenance dgn-np:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_provenance;
    np:hasPublicationInfo dgn-np:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_assertion a np:Assertion .
  
  dgn-np:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_provenance a np:Provenance .
  
  dgn-np:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0029458 a ncit:C7057 .
  
  dgn-gda:DGN42a7e1bc8740bac909027d4e004170aa sio:SIO_000628 miriam-gene:1756, lld:C0029458;
    a sio:SIO_001121 .
}

dgn-np:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_provenance {
  dgn-np:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_assertion dcterms:description
      "[We conclude that in this large population sample the (TA)(n) dinucleotide repeat polymorphism at the 5' end of the ERalpha gene accounts for part of the heritable component of BMD and might prove useful in the prediction of vertebral fracture risk in postmenopausal 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:10942433;
    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:NP662749.RATxqQZQPJqP8vOwk5c7AlyN_ru0GJBNXQ-sBoYxfEFfY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:40+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" .
}