Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_assertion> ?p ?o ?g. }
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- NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_assertion type Assertion NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_head.
- NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_assertion wasGeneratedBy ECO_0000203 NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_provenance.
- NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_assertion wasDerivedFrom befree-20140225 NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_provenance.
- NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_assertion SIO_000772 17276182 NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_provenance.
- NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_assertion evidence source_evidence_literature NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_provenance.
- NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_assertion description "[One missense KCNQ1 mutation, R14C, was identified in 1 family with a high prevalence of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476399.RAvUMZMtN42GmIHvOTToWID-CGFZfd_pRehDaZfaiA2co130_provenance.