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- source_evidence_literature type ECO_0000212 NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.
- NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.
- NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_assertion evidence source_evidence_literature NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.
- NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_assertion SIO_000772 18309337 NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.
- NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_assertion wasDerivedFrom befree-20150227 NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.
- NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_assertion wasGeneratedBy ECO_0000203 NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320882.RAMKl6dxudYpGAJ4psYEjPQXUseYldt45rzfjX_DOD6yQ130_provenance.