Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP92759.RAnfsjTIMarbn0iXsre7VqST_a2hAbA3O2yWdTzWbZbFI#assertion> ?p ?o ?g. }
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- assertion description "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
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- assertion SIO_000772 15174025 provenance.
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