Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_assertion> ?p ?o ?g. }
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- NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_assertion type Assertion NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_head.
- NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_assertion wasGeneratedBy ECO_0000203 NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_provenance.
- NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_assertion wasDerivedFrom befree-20140225 NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_provenance.
- NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_assertion SIO_000772 17309881 NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_provenance.
- NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_assertion evidence source_evidence_literature NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_provenance.
- NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_assertion description "[Rett syndrome (RTT) is an X-linked neurodevelopmental disorder linked to heterozygous de novo mutations in the MECP2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_provenance.