Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_assertion type Assertion NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_head.
- NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_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." NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_provenance.
- NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_assertion evidence source_evidence_curated NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_provenance.
- NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_assertion SIO_000772 15863612 NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_provenance.
- NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_assertion wasDerivedFrom uniprot-2016 NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_provenance.
- NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_assertion wasGeneratedBy ECO_0000218 NP4018.RAWTwk4nKaZligYj0P9y_eVvEFt3McwRevHWITmAMVM1k130_provenance.