Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion> ?p ?o ?g. }
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- NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion type Assertion NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_head.
- NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion description "[A number of animal models with complete or partial lack of MeCP2 functions have been generated to correlate the clinical phenotype of Rett syndrome, and studies involving different mutations of MeCP2 have shown similar effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_provenance.
- NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion evidence source_evidence_literature NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_provenance.
- NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion SIO_000772 23912219 NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_provenance.
- NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion wasDerivedFrom befree-2016 NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_provenance.
- NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion wasGeneratedBy ECO_0000203 NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_provenance.