Matches in Nanopublications for { ?s ?p "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP691184.RACNNCAc_lr4AMVTeUKo8cj_TLqGMvUdGBi6uvOH38bmI130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691184.RACNNCAc_lr4AMVTeUKo8cj_TLqGMvUdGBi6uvOH38bmI130_provenance.
- NP203664.RAMAf1bcFIRDnzvnBpQ9t7gBNFSazIOMk852L2PlL8m1Q130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203664.RAMAf1bcFIRDnzvnBpQ9t7gBNFSazIOMk852L2PlL8m1Q130_provenance.
- assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.
- assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1260050.RALTFBRn7drvt2G6aa113XVqV_DOk3PYpuHhHB_n4CkU8130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260050.RALTFBRn7drvt2G6aa113XVqV_DOk3PYpuHhHB_n4CkU8130_provenance.
- NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260053.RAHmDjl-guvlKeEot3CanW-aigt7gR7ToJtdChocGojjg130_provenance.
- NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260049.RA8bkmcyN0kwUw599Ojb7Y0yA90t5IhotDxVzvWCNS1sE130_provenance.
- NP1260054.RA6MDinv-CZuFpODiqFEuRCoMyPozcW3hrWdEaJ-87zKc130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260054.RA6MDinv-CZuFpODiqFEuRCoMyPozcW3hrWdEaJ-87zKc130_provenance.