@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU> .
@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:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_head {
  this: np:hasAssertion dgn-np:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_assertion;
    np:hasProvenance dgn-np:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_provenance;
    np:hasPublicationInfo dgn-np:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_assertion a np:Assertion .
  
  dgn-np:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_provenance a np:Provenance .
  
  dgn-np:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_assertion {
  miriam-gene:1540 a ncit:C16612 .
  
  lld:C0029410 a ncit:C7057 .
  
  dgn-gda:DGNd60bbc72fdf5c2efbf6b9a4287c4b3ab sio:SIO_000628 miriam-gene:1540, lld:C0029410;
    a sio:SIO_001121 .
}

dgn-np:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_provenance {
  dgn-np:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_assertion dcterms:description
      "[A genetic contribution to THR for OA was assessed by 1) identifying familial clusters of OA patients with THR, 2) applying the minimum founder test (MFT) to estimate the minimum number of ancestors (`founders`) that would account for the genealogy of all 2,713 patients with THR for OA, compared with the average number of founders for control lists, 3) calculating an average pairwise kinship coefficient (KC) for the patient list and control lists, and 4) estimating the relative risk (RR) for THR among relatives of OA patients who have undergone the procedure.]. 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:11145037;
    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:NP556316.RAv7Z7am9px1pKa0DrYNmeYlmCNXEGoEe8opm_O0jTpnU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:35+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" .
}