Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_assertion> ?p ?o ?g. }
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- NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_assertion type Assertion NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_head.
- NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_assertion wasGeneratedBy ECO_0000203 NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_provenance.
- NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_assertion wasDerivedFrom befree-20150227 NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_provenance.
- NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_assertion SIO_000772 24842605 NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_provenance.
- NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_assertion evidence source_evidence_literature NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_provenance.
- NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_assertion description "[SCN1A mutation may be a clinically-useful genetic marker in order to distinguish GEFS+ patients from those with classic idiopathic generalised epilepsy, even if they present an atypical clinical picture.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682474.RAReb7gNwrWsxxc3tthV50_ynRmt5Uv399zKHKptki0Tc130_provenance.