@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg> .
@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:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_head {
  this: np:hasAssertion dgn-np:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_assertion;
    np:hasProvenance dgn-np:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_provenance;
    np:hasPublicationInfo dgn-np:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_assertion a np:Assertion .
  
  dgn-np:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_provenance a np:Provenance .
  
  dgn-np:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_assertion {
  miriam-gene:4049 a ncit:C16612 .
  
  lld:C0029456 a ncit:C7057 .
  
  dgn-gda:DGNabf684b6d555d122e4b72e444f1d25c2 sio:SIO_000628 miriam-gene:4049, lld:C0029456;
    a sio:SIO_001121 .
}

dgn-np:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_provenance {
  dgn-np:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_assertion dcterms:description
      "[TNF-alpha T(-1031)C, TNF-beta A252G, and TNFRII A1663G polymorphisms may be genetic factors for osteoporosis in Korean postmenopausal women, and the TNFRII T676G and C1690T polymorphisms and their combined polymorphism affected serum sTNFRII levels.]. 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:19369902;
    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:NP609937.RAO0GyqQ9fvu0bR9ThhFeXrMQoh1v3aMNm9gzjIZuALMg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:06+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" .
}