Matches in Nanopublications for { ?s ?p "[Cohen syndrome (CS) is a rare autosomal recessive condition caused by mutations and/or large rearrangements in the VPS13B gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP182819.RAgyppEUJPg_Fdjve_InYy1RgvidN-U0UqLIwz28fBD6Q130_assertion description "[Cohen syndrome (CS) is a rare autosomal recessive condition caused by mutations and/or large rearrangements in the VPS13B gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182819.RAgyppEUJPg_Fdjve_InYy1RgvidN-U0UqLIwz28fBD6Q130_provenance.
- assertion description "[Cohen syndrome (CS) is a rare autosomal recessive condition caused by mutations and/or large rearrangements in the VPS13B gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP976704.RAMVU3H7RyCivHxvP610BpvczmI05NjzO-aZE2rpdD3QE130_assertion description "[Cohen syndrome (CS) is a rare autosomal recessive condition caused by mutations and/or large rearrangements in the VPS13B gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976704.RAMVU3H7RyCivHxvP610BpvczmI05NjzO-aZE2rpdD3QE130_provenance.
- NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_assertion description "[Cohen syndrome (CS) is a rare autosomal recessive condition caused by mutations and/or large rearrangements in the VPS13B gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_provenance.