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- source_evidence_literature type ECO_0000212 NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_provenance.
- NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_assertion description "[This study reaffirms the view that large MECP2 deletions are an important cause of both classical and atypical RTT syndrome, and cautions that apparent deletions detected using high-throughput diagnostic techniques require further characterisation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_provenance.
- NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_assertion evidence source_evidence_literature NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_provenance.
- NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_assertion SIO_000772 17712354 NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_provenance.
- NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_assertion wasDerivedFrom befree-2016 NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_provenance.
- NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_assertion wasGeneratedBy ECO_0000203 NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_provenance.