Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion description "[It is now clearly emerging that epilepsy has distinctive characteristics in typical Rett syndrome and in the different syndromes caused by CDKL5 and FOXG1 gene alterations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion evidence source_evidence_literature NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion SIO_000772 22998673 NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion wasDerivedFrom befree-2016 NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion wasGeneratedBy ECO_0000203 NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- befree-2016 importedOn "2016-02-19" NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.