Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_assertion> ?p ?o ?g. }
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- NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_assertion type Assertion NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_head.
- NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_assertion wasGeneratedBy ECO_0000203 NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_provenance.
- NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_assertion wasDerivedFrom befree-20140225 NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_provenance.
- NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_assertion SIO_000772 18398334 NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_provenance.
- NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_assertion evidence source_evidence_literature NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_provenance.
- NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_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." NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_provenance.