Matches in Nanopublications for { ?s ?p "[Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_assertion description "[Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294791.RAHSGMkmogiv8ybmgF-2LEPSd-U2UGSrP2f-3KngBk3dA130_provenance.
- NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_assertion description "[Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.