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- source_evidence_literature type ECO_0000212 NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_provenance.
- NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_assertion description "[Mutations in the Norrie Disease gene, Norrie Disease Pseudoglioma (NDP) lead to a phenotypically heterogeneous group of retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_provenance.
- NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_assertion evidence source_evidence_literature NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_provenance.
- NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_assertion SIO_000772 19373682 NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_provenance.
- NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_assertion wasDerivedFrom befree-20140225 NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_provenance.
- NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_assertion wasGeneratedBy ECO_0000203 NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP870262.RAGm29gDTOa3rRDk5_Dlk-p_mjV8S9lVqK_kF-bK2Wbnk130_provenance.