Matches in Nanopublications for { ?s ?p "[Our findings suggest that SCN1A mutations may cause susceptibility to an idiopathic focal epilepsy phenotype, the final phenotype depending on other (genetic or nongenetic) factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 3 of
3
with 100 items per page.
- NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_assertion description "[Our findings suggest that SCN1A mutations may cause susceptibility to an idiopathic focal epilepsy phenotype, the final phenotype depending on other (genetic or nongenetic) factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766147.RA9FxhmnqwsCx4SEba7qwnnkqk6f9d1tkM_epPz6qvzIE130_provenance.
- NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_assertion description "[Our findings suggest that SCN1A mutations may cause susceptibility to an idiopathic focal epilepsy phenotype, the final phenotype depending on other (genetic or nongenetic) factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_provenance.
- NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_assertion description "[Our findings suggest that SCN1A mutations may cause susceptibility to an idiopathic focal epilepsy phenotype, the final phenotype depending on other (genetic or nongenetic) factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_provenance.