Matches in Nanopublications for { ?s ?p "[Congenital hypothyroidism (CH) due to thyroglobulin (TG) deficit is an autosomal recessive disease (OMIM #274700) characterized by hypothyroidism, goiter, low serum TG, and a negative perchlorate discharge test.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 3 of
3
with 100 items per page.
- assertion description "[Congenital hypothyroidism (CH) due to thyroglobulin (TG) deficit is an autosomal recessive disease (OMIM #274700) characterized by hypothyroidism, goiter, low serum TG, and a negative perchlorate discharge test.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1057323.RAi1AqqDCgkHKXqOOSQq3BBUj__rj6vvnQzIu-Xhm8wBI130_assertion description "[Congenital hypothyroidism (CH) due to thyroglobulin (TG) deficit is an autosomal recessive disease (OMIM #274700) characterized by hypothyroidism, goiter, low serum TG, and a negative perchlorate discharge test.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1057323.RAi1AqqDCgkHKXqOOSQq3BBUj__rj6vvnQzIu-Xhm8wBI130_provenance.
- NP730820.RAK9W5CWPnO7nkAFvr2v7ZrJ5uip1173-bBcvDtDCnh0E130_assertion description "[Congenital hypothyroidism (CH) due to thyroglobulin (TG) deficit is an autosomal recessive disease (OMIM #274700) characterized by hypothyroidism, goiter, low serum TG, and a negative perchlorate discharge test.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP730820.RAK9W5CWPnO7nkAFvr2v7ZrJ5uip1173-bBcvDtDCnh0E130_provenance.