Matches in Nanopublications for { ?s ?p "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631416.RAGfERsR_l6fQSkUmVEGV-Md73jwW4r3l633SsC4u6uWo130_provenance.
- assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425263.RAnkhHLRU6kJJ6W3JMmC6uihmOFohajatwM5qvb868MQ4130_provenance.
- NP374770.RA6jydFshdAkWHobD5CuKFQiewNW9O7mX_QCdmmEZ88B8130_assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374770.RA6jydFshdAkWHobD5CuKFQiewNW9O7mX_QCdmmEZ88B8130_provenance.
- NP425248.RAELnh6omxC_K3CtlMdtGj3WRMk09wwLpwD-2yiXyFyRs130_assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425248.RAELnh6omxC_K3CtlMdtGj3WRMk09wwLpwD-2yiXyFyRs130_provenance.
- NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_assertion description "[Mutations of the transforming growth factor beta (TGFbeta) receptor components ENDOGLIN and ALK-1 cause the autosomal dominant vascular disorder hereditary haemorrhagic telangiectasia (HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP732556.RA9yue_PzywYPwTBAxFWBIJZv9blU5EgJWAGbqgRF7DI8130_provenance.