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- NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_assertion type Assertion NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_head.
- NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_assertion wasGeneratedBy ECO_0000203 NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_provenance.
- NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_assertion wasDerivedFrom befree-20140225 NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_provenance.
- NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_assertion SIO_000772 18398334 NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_provenance.
- NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_assertion evidence source_evidence_literature NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_provenance.
- NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_provenance.