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- source_evidence_literature type ECO_0000212 NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.
- NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_assertion description "[These RNF168-dependent chromatin modifications orchestrate the accumulation of 53BP1 and BRCA1 to DNA lesions, and their loss is the likely cause of the cellular and developmental phenotypes associated with RIDDLE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.
- NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_assertion evidence source_evidence_literature NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.
- NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_assertion SIO_000772 19203578 NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.
- NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_assertion wasDerivedFrom befree-20150227 NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.
- NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_assertion wasGeneratedBy ECO_0000203 NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.