Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.
- NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_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." NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.
- NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_assertion evidence source_evidence_literature NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.
- NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_assertion SIO_000772 22998673 NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.
- NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_assertion wasDerivedFrom befree-20140225 NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.
- NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_assertion wasGeneratedBy ECO_0000203 NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP258982.RAuvXyEVxpZ6aci6SQul1znlHZ-DFhYs2V1elKfjchff8130_provenance.