Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion wasGeneratedBy ECO_0000203 NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion wasDerivedFrom befree-2016 NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion SIO_000772 22998673 NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_assertion evidence source_evidence_literature NP1014878.RA-o2AiREI8aTVFm6qbiD2FW7MsB5cJblB_EkesKvm6sc130_provenance.
- 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.