@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E> .
@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:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_head {
  this: np:hasAssertion dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_assertion;
    np:hasProvenance dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_provenance;
    np:hasPublicationInfo dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_assertion a np:Assertion .
  
  dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_provenance a np:Provenance .
  
  dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0747079 a ncit:C7057 .
  
  dgn-gda:DGN5755a41bc8f68f69b5c62d13f1a04c09 sio:SIO_000628 miriam-gene:1756, lld:C0747079;
    a sio:SIO_001121 .
}

dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_provenance {
  dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_assertion dcterms:description
      "[As several non-synonymous single nucleotide polymorphisms (SNPs) have been identified within the P2Y(2) receptor gene in humans, we examined associations between genetic variations in the P2Y(2) receptor gene and bone mineral density (BMD) (i.e., osteoporosis risk), in a cohort of fracture patients.]. 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:22773251;
    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:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:36+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" .
}