@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc> .
@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:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_head {
  this: np:hasAssertion dgn-np:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_assertion;
    np:hasProvenance dgn-np:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_provenance;
    np:hasPublicationInfo dgn-np:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_assertion a np:Assertion .
  
  dgn-np:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_provenance a np:Provenance .
  
  dgn-np:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_assertion {
  miriam-gene:7439 a ncit:C16612 .
  
  lld:C0005940 a ncit:C7057 .
  
  dgn-gda:DGN8415e52d101b0a7c8367787204236141 sio:SIO_000628 miriam-gene:7439, lld:C0005940;
    a sio:SIO_001121 .
}

dgn-np:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_provenance {
  dgn-np:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_assertion dcterms:description
      "[This study shows for the first time that the polymorphisms polyAla and Pro198Leu of the GPX1 gene, individually and in combination, are associated with BMD and therefore may be useful as genetic markers for bone disease.]. 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:21045266;
    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:NP480056.RAr2ppn0wSD01eolvl8gGNWCQPlP99N63FzGQVTCuAZlc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:47+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" .
}