Matches in Nanopublications for { ?s ?p "[The hereditary hemorrhagic telangiectasia family is caused by a 145delG mutation of ACVRL1 gene, resulting in frameshift and a new stop codon at codon 53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The hereditary hemorrhagic telangiectasia family is caused by a 145delG mutation of ACVRL1 gene, resulting in frameshift and a new stop codon at codon 53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP152704.RAacPI9qIOXBgMS5UZhDE4UK73JHEGA6QLUDhIvChejDg130_assertion description "[The hereditary hemorrhagic telangiectasia family is caused by a 145delG mutation of ACVRL1 gene, resulting in frameshift and a new stop codon at codon 53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152704.RAacPI9qIOXBgMS5UZhDE4UK73JHEGA6QLUDhIvChejDg130_provenance.
- NP215818.RAq-67oG3t0pRECenYQTASQe0qlK3Jij_V5kATE_PRD7s130_assertion description "[The hereditary hemorrhagic telangiectasia family is caused by a 145delG mutation of ACVRL1 gene, resulting in frameshift and a new stop codon at codon 53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215818.RAq-67oG3t0pRECenYQTASQe0qlK3Jij_V5kATE_PRD7s130_provenance.
- NP238685.RAyubfNtu8S8hy06r5SQ6cu2IdHb4ZaVDBYga3UBH-AV0130_assertion description "[The hereditary hemorrhagic telangiectasia family is caused by a 145delG mutation of ACVRL1 gene, resulting in frameshift and a new stop codon at codon 53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238685.RAyubfNtu8S8hy06r5SQ6cu2IdHb4ZaVDBYga3UBH-AV0130_provenance.