Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_assertion> ?p ?o ?g. }
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- NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_assertion type Assertion NP626208.RAtAsXZNrtnluhqkaLLGRX7W_YvBvTtWjjggdJrnNPpqQ130_head.
- 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.