Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_assertion> ?p ?o ?g. }
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- NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_assertion type Assertion NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_head.
- NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_assertion description "[These data indicate that gain-of-function mutations of CaV1.2 exons 8 and 8A cause distinct forms of TS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_provenance.
- NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_assertion evidence source_evidence_literature NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_provenance.
- NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_assertion SIO_000772 15863612 NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_provenance.
- NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_assertion wasDerivedFrom befree-2016 NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_provenance.
- NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_assertion wasGeneratedBy ECO_0000203 NP492369.RAVQqYR1mAbqzDHEA1XHtE3f1mBFRO_Q5S29SKl3lPi5k130_provenance.