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- NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_assertion type Assertion NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_head.
- 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.
- NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_assertion evidence source_evidence_literature NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_provenance.
- NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_assertion SIO_000772 19339291 NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_provenance.
- NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_assertion wasDerivedFrom befree-2016 NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_provenance.
- NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_assertion wasGeneratedBy ECO_0000203 NP729971.RAqyb1tkxBCKyjmzLXuX7wc-e1lRVfJusEjJQm7ZrO_8s130_provenance.