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- source_evidence_literature type ECO_0000212 NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.
- NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_assertion description "[Cockayne's Syndrome (CS) is a rare autosomal recessive disorder characterized by deficiency in the transcription-couple DNA repair pathway caused by mutations in the genes ERCC6 in 65% of individuals and ERCC8 in 35% of individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.
- NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_assertion evidence source_evidence_literature NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.
- NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_assertion SIO_000772 26721046 NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.
- NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_assertion wasDerivedFrom befree-2016 NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.
- NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_assertion wasGeneratedBy ECO_0000203 NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.