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- NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_assertion type Assertion NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_head.
- NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_provenance.
- NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_assertion evidence source_evidence_literature NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_provenance.
- NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_assertion SIO_000772 11739564 NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_provenance.
- NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_assertion wasDerivedFrom befree-20140225 NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_provenance.
- NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_assertion wasGeneratedBy ECO_0000203 NP874115.RArbCKif4oNYaizmurqqw3Vc4Fj197kBHdWxit3GTN2Es130_provenance.