Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_assertion> ?p ?o ?g. }
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- NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_assertion type Assertion NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_head.
- NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_assertion description "[Mutations in methyl CpG binding protein 2 (MECP2) are identified in most patients with classic Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_provenance.
- NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_assertion evidence source_evidence_literature NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_provenance.
- NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_assertion SIO_000772 19623215 NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_provenance.
- NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_assertion wasDerivedFrom befree-2016 NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_provenance.
- NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_assertion wasGeneratedBy ECO_0000203 NP752802.RAbj9j1lcKbpaSmfXrWnwF2wcFLLkwIgw6SXO9MVUFhKY130_provenance.