Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_assertion> ?p ?o ?g. }
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- NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_assertion type Assertion NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_head.
- NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_assertion wasGeneratedBy ECO_0000203 NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_provenance.
- NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_assertion wasDerivedFrom befree-2016 NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_provenance.
- NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_assertion SIO_000772 22998673 NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_provenance.
- NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_assertion evidence source_evidence_literature NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_provenance.
- NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_assertion description "[Diagnostic criteria have been modified only slightly over time, even after discovering that MECP2 gene alterations are present in >90% of patients with typical Rett syndrome but only in 50-70% of atypical cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014886.RAv2Bd30CS03z0eD7wF6c_EwAE_zJHenPs1P5HF1Miq6Q130_provenance.