@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_head {
  this: np:hasAssertion dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_assertion;
    np:hasProvenance dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_provenance;
    np:hasPublicationInfo dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_assertion a np:Assertion .
  
  dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_provenance a np:Provenance .
  
  dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_assertion {
  miriam-gene:2487 a ncit:C16612 .
  
  lld:C0029408 a ncit:C7057 .
  
  dgn-gda:DGNb08b27214564b3a6f21db713329ef9e3 sio:SIO_000628 miriam-gene:2487, lld:C0029408;
    a sio:SIO_001122 .
}

dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_provenance {
  dgn-np:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_assertion dcterms:description
      "[Our data confirm findings of another study, that a rare haplotype with both Arg200Trp and Arg324Gly FRZB variants contributes to the genetic susceptibility to hip OA among Caucasian women, and that these polymorphisms may contribute to increased serum levels of proteins as biomarkers of 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:16572458;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP542589.RAJJpO8dKVdPD6766bWeqW-3rODlVocprawGCwBHhnMOg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:50+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}