Matches in Nanopublications for { ?s ?p "[Loss-of-function germline mutations of the RET proto-oncogene are reported in familial and sporadic cases of Hirschsprung disease (HSCR) with a variable frequency ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP202034.RA-d3DIeITWzmNE2_lacZXjSCEdSgXhm5sMBM7Tvf0Xxs130_assertion description "[Loss-of-function germline mutations of the RET proto-oncogene are reported in familial and sporadic cases of Hirschsprung disease (HSCR) with a variable frequency ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP202034.RA-d3DIeITWzmNE2_lacZXjSCEdSgXhm5sMBM7Tvf0Xxs130_provenance.