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- NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_assertion type Assertion NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_head.
- NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_assertion wasGeneratedBy ECO_0000203 NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_provenance.
- NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_assertion wasDerivedFrom befree-2016 NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_provenance.
- NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_assertion SIO_000772 24646837 NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_provenance.
- NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_assertion evidence source_evidence_literature NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_provenance.
- NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_assertion description "[In 2009, we presented a kindred with FHM due to the L263V SCN1A mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1165427.RAiu6wV_F6gKGwSjM9aHRuv-GB2xl3oyghVn409O1B_zA130_provenance.