@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM> .
@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:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_head {
  this: np:hasAssertion dgn-np:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_assertion;
    np:hasProvenance dgn-np:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_provenance;
    np:hasPublicationInfo dgn-np:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_assertion a np:Assertion .
  
  dgn-np:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_provenance a np:Provenance .
  
  dgn-np:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_assertion {
  miriam-gene:81034 a ncit:C16612 .
  
  lld:C0029410 a ncit:C7057 .
  
  dgn-gda:DGNf28c4307535ebc0d517613f1a271bc3c sio:SIO_000628 miriam-gene:81034, lld:C0029410;
    a sio:SIO_001121 .
}

dgn-np:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_provenance {
  dgn-np:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_assertion dcterms:description
      "[The genetic contribution to THR for OA was assessed by (a) identifying familial clusters of THR for OA, (b) applying the minimum founder test (MFT) to estimate the minimum number of ancestors to account for all patients with THR for OA, compared to the average number of founders for control lists, (c) calculating an average pairwise kinship coefficient (KC) for the patient and control lists, (d) estimating the relative risk (RR) for relatives of patients with THR for OA.]. 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:11338422;
    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:NP701426.RA4Bizchm9vBArMx7lSh8dnje6u28TBNR61TcyNTi3GmM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:06+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" .
}