Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_assertion> ?p ?o ?g. }
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- NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_assertion type Assertion NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_head.
- NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_assertion wasGeneratedBy ECO_0000203 NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_provenance.
- NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_assertion wasDerivedFrom befree-20150227 NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_provenance.
- NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_assertion SIO_000772 18021921 NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_provenance.
- NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_assertion evidence source_evidence_literature NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_provenance.
- NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_assertion description "[Although SCN1A, the gene encoding the neuronal voltage-gated sodium channel, type 1A, is a well-recognized target of mutations underlying a spectrum of epilepsy syndromes, and lies within an extended 12-Mb disease-associated haplotype at the familial hemiplegic migraine-3 locus, it remains to be confirmed that mutations within this gene itself cause syndromes that include migraine phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682455.RAub7jz9m01sFdwpqaF2y19Dff1t6TCchB8TPLijxGve4130_provenance.