Matches in Nanopublications for { ?s ?p "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP141132.RAcXlkZjR6D9kmi9qS3tN2y744XeJBumeQrKl2NnrzuqY130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141132.RAcXlkZjR6D9kmi9qS3tN2y744XeJBumeQrKl2NnrzuqY130_provenance.
- NP175364.RASqBaaEwmbSIEBA8cOYd9TPvWbm-5fuu9S72qMjC1gWM130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP175364.RASqBaaEwmbSIEBA8cOYd9TPvWbm-5fuu9S72qMjC1gWM130_provenance.
- NP146039.RAY08lZkkVS17uB7Do51J3qN5Djz6wmBx6qAibFEgTC74130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146039.RAY08lZkkVS17uB7Do51J3qN5Djz6wmBx6qAibFEgTC74130_provenance.
- NP533675.RAr4Q97y7VBHUPJAET1NbhQrG1XYaQWH9V2RCxK8N4DW4130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533675.RAr4Q97y7VBHUPJAET1NbhQrG1XYaQWH9V2RCxK8N4DW4130_provenance.
- NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_provenance.
- assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP245388.RAWwRRGtN_JNuiYo0xmn-EJv-BDune2W_9C627UeT3a5A130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245388.RAWwRRGtN_JNuiYo0xmn-EJv-BDune2W_9C627UeT3a5A130_provenance.
- NP718934.RAlmxJmhdMRrZfLBAYPXDPdqT_mN6H6_s5Nx7kZzLKZEo130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718934.RAlmxJmhdMRrZfLBAYPXDPdqT_mN6H6_s5Nx7kZzLKZEo130_provenance.
- NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.
- NP697713.RA8Tf_mZefaNHVOQa6xWbM5x4_p0cdMz-5EmNtNHyLGhc130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697713.RA8Tf_mZefaNHVOQa6xWbM5x4_p0cdMz-5EmNtNHyLGhc130_provenance.
- NP245389.RA4qBOijhHuZSbfqkwNofKbbdrm2Rct5AvVrerhA710sI130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245389.RA4qBOijhHuZSbfqkwNofKbbdrm2Rct5AvVrerhA710sI130_provenance.