Matches in Nanopublications for { ?s ?p "[Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP5512.RASO2cgStmLLIwpKyQsNG7L2NhhZb4RhGvcupnEdXCGHU130_assertion description "[Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5512.RASO2cgStmLLIwpKyQsNG7L2NhhZb4RhGvcupnEdXCGHU130_provenance.