Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_assertion type Assertion NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_head.
- NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_assertion wasGeneratedBy ECO_0000203 NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_provenance.
- NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_assertion wasDerivedFrom befree-20150227 NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_provenance.
- NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_assertion SIO_000772 15537666 NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_provenance.
- NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_assertion evidence source_evidence_literature NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_provenance.
- NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_assertion description "[All five probands with familial disease had a deletion mutation within the closely linked STX16 gene and a GNAS imprinting defect involving only the exon 1A region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429815.RASK3dt4iTQ6EcOPh1p88J08Y_4ukj1X0nekVrmr8IosQ130_provenance.