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- source_evidence_literature type ECO_0000212 NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_provenance.
- NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_assertion description "[The fragment was used to search for mutations of the corresponding gamma-cGMP-PDE gene in patients with autosomal dominant, autosomal recessive, or isolate case retinitis pigmentosa, and Usher's syndrome type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_provenance.
- NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_assertion evidence source_evidence_literature NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_provenance.
- NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_assertion SIO_000772 1683837 NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_provenance.
- NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_assertion wasDerivedFrom befree-20140225 NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_provenance.
- NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_assertion wasGeneratedBy ECO_0000203 NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP210414.RAhCnHptgQg6VkKL-zJ0xx7Bba7jfmeHjz5M7mU7xCQvY130_provenance.