@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME> .
@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:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_head {
  this: np:hasAssertion dgn-np:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_assertion ;
    np:hasProvenance dgn-np:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_provenance ;
    np:hasPublicationInfo dgn-np:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_assertion a np:Assertion .
  dgn-np:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_provenance a np:Provenance .
  dgn-np:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_assertion {
  miriam-gene:344875 a ncit:C16612 .
  lld:C0409959 a ncit:C7057 .
  dgn-gda:DGN0472960f9cd7108293416e76e61edaf6 sio:SIO_000628 miriam-gene:344875 , lld:C0409959 ;
    a sio:SIO_001121 .
}
dgn-np:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_provenance {
  dgn-np:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_assertion dcterms:description "[Six polymorphisms in GDF5, PTGS2, 7q22 locus, DVWA, DIO3, and ASPN that have been associated with knee OA were analyzed in 255 patients that had undergone total knee replacement (TKR) because of primary OA and in 457 healthy controls.]. 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:22102359 ;
    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:NP812206.RADV0Ns7DPis_PbEhFuwWvrQfssuW_wcQ__P0UUR7nQME130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:18+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 ;
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}