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- NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_assertion type Assertion NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_head.
- NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_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." NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_provenance.
- NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_assertion evidence source_evidence_literature NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_provenance.
- NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_assertion SIO_000772 22998673 NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_provenance.
- NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_assertion wasDerivedFrom befree-2016 NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_provenance.
- NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_assertion wasGeneratedBy ECO_0000203 NP1014885.RArU1yVgTLrfySM1KpO4G1uX3w2veYL8hjDAo1KC-cnB0130_provenance.