Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.
• assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.
• NP374806.RAdNLREfHFUa-sQN7XxOauTAHRa_xPVI3_k7In8prBD1I130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374806.RAdNLREfHFUa-sQN7XxOauTAHRa_xPVI3_k7In8prBD1I130_provenance.
• NP532308.RAdOFDE8X1ybJ9xeN9_IGvnB4sdEN74yU9rs75uYivtXk130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532308.RAdOFDE8X1ybJ9xeN9_IGvnB4sdEN74yU9rs75uYivtXk130_provenance.
• NP532309.RASQtg4z284ur9nIB-R2XUqBxIHYEWhSrDY4UVfD3Ifog130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532309.RASQtg4z284ur9nIB-R2XUqBxIHYEWhSrDY4UVfD3Ifog130_provenance.
• NP222401.RAC-_a5Wy45DOw0YTb3dbHRQug91lkY8FEEOWhWEtpv1k130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222401.RAC-_a5Wy45DOw0YTb3dbHRQug91lkY8FEEOWhWEtpv1k130_provenance.
• NP222373.RAKfTT8qsGRWIpj8U3uqDApPLbloGTAsGUS6jYvaCjPVE130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222373.RAKfTT8qsGRWIpj8U3uqDApPLbloGTAsGUS6jYvaCjPVE130_provenance.
• NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.
• NP532306.RAMYN5KLcxTqFaQc8wID-UeI_rts7ycJClWZqNUencRg0130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532306.RAMYN5KLcxTqFaQc8wID-UeI_rts7ycJClWZqNUencRg0130_provenance.
• NP532305.RAzkdZTTs6gYx2cZqhXGigNtVfePTVmPvYiBQIg7Nd2gw130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532305.RAzkdZTTs6gYx2cZqhXGigNtVfePTVmPvYiBQIg7Nd2gw130_provenance.
• NP532307.RA7ljT2jzyMeOst8eKEChGqITzBs9IvmG-oWDOlZFUcK4130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532307.RA7ljT2jzyMeOst8eKEChGqITzBs9IvmG-oWDOlZFUcK4130_provenance.
• NP532310.RA5OAviw0sjzRtkaGCyeOUXC7ecF1KTxkIbtmahqdqyu0130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532310.RA5OAviw0sjzRtkaGCyeOUXC7ecF1KTxkIbtmahqdqyu0130_provenance.