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http://bio2rdf.org/geneid:55835 http://rdf.biosemantics.org/vocabularies/gene_disease_nanopub_example#RAb5oaamdOKxwOjo1Y3wogV_xSwsmjl-uTfciTSncoUCs.Association_1 http://semanticscience.org/resource/refers-to http://bio2rdf.org/omim:210600 http://rdf.biosemantics.org/vocabularies/gene_disease_nanopub_example#RAb5oaamdOKxwOjo1Y3wogV_xSwsmjl-uTfciTSncoUCs.Association_1 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/statistical-association http://rdf.biosemantics.org/vocabularies/gene_disease_nanopub_example#RAb5oaamdOKxwOjo1Y3wogV_xSwsmjl-uTfciTSncoUCs.Association_1 http://www.w3.org/2000/01/rdf-schema#comment This association has p-value of 0.00066, has attribute gene CENPJ (Entrenz gene id 55835) and attribute disease Seckel Syndrome (OMIM 210600). http://rdf.biosemantics.org/vocabularies/gene_disease_nanopub_example#RAb5oaamdOKxwOjo1Y3wogV_xSwsmjl-uTfciTSncoUCs.Association_1_p_value http://semanticscience.org/resource/has-value 0.0000656211037469712 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