Matches in Nanopublications for { ?s ?p "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP351402.RAlPTSqV3OWjnSDNeaQD4zQZmvbppydVrKc7FriWRCnvg130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351402.RAlPTSqV3OWjnSDNeaQD4zQZmvbppydVrKc7FriWRCnvg130_provenance.
- NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.
- NP222849.RA8xVnwER1mnK7Ji_Reqk8OIz4QXjkWUew_ubksWQrY0g130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222849.RA8xVnwER1mnK7Ji_Reqk8OIz4QXjkWUew_ubksWQrY0g130_provenance.
- NP822078.RAU3sN1VNRLrZQNuPur8HiMCznWo8TbG1IGK2eRgZdaKU130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822078.RAU3sN1VNRLrZQNuPur8HiMCznWo8TbG1IGK2eRgZdaKU130_provenance.
- NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_provenance.
- NP739277.RAFeSp8Qv7qTxEwXQ329faxDf97TAVcgyUcHaLWJxhGXA130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739277.RAFeSp8Qv7qTxEwXQ329faxDf97TAVcgyUcHaLWJxhGXA130_provenance.
- assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822076.RAIrpNtbVODaDsHBGjXr2y3PdjJxRSBMgX8jeXS48zj1Q130_provenance.