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- NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_assertion type Assertion NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_head.
- 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.
- NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_assertion evidence source_evidence_literature NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_provenance.
- NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_assertion SIO_000772 19339291 NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_provenance.
- NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_assertion wasDerivedFrom befree-20150227 NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_provenance.
- NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_assertion wasGeneratedBy ECO_0000203 NP682390.RAuc-PBtFHaR4_HsiWWixkRsWiDs7mYhHWYuYkXtcXEuU130_provenance.