Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion> ?p ?o ?g. }
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- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion type Assertion NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_head.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion evidence source_evidence_literature NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion SIO_000772 22998673 NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion wasDerivedFrom befree-2016 NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion wasGeneratedBy ECO_0000203 NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.