Matches in Nanopublications for { ?s ?p "[These findings expand the number of APP mutations linked to hereditary cerebral hemorrhage with amyloidosis, reinforcing the link between this phenotype and codon 693 of APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_assertion description "[These findings expand the number of APP mutations linked to hereditary cerebral hemorrhage with amyloidosis, reinforcing the link between this phenotype and codon 693 of APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133373.RAYI2Zu1c1lGtfI2a8hRg53jxIP5F5Sw2eVuDbrtA8SEs130_provenance.
- NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_assertion description "[These findings expand the number of APP mutations linked to hereditary cerebral hemorrhage with amyloidosis, reinforcing the link between this phenotype and codon 693 of APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133374.RAb3P6khvNv7rmy6a-fuGJkL2JD6RRuoVl25GfReqJU-E130_provenance.
- assertion description "[These findings expand the number of APP mutations linked to hereditary cerebral hemorrhage with amyloidosis, reinforcing the link between this phenotype and codon 693 of APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These findings expand the number of APP mutations linked to hereditary cerebral hemorrhage with amyloidosis, reinforcing the link between this phenotype and codon 693 of APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP183436.RAzX0FuKwYteOWRaudz0zUXVoSHg4tu0w5j2F7DLMRT10130_assertion description "[These findings expand the number of APP mutations linked to hereditary cerebral hemorrhage with amyloidosis, reinforcing the link between this phenotype and codon 693 of APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183436.RAzX0FuKwYteOWRaudz0zUXVoSHg4tu0w5j2F7DLMRT10130_provenance.
- NP183435.RAuqLxfW3v8ZLySRRc_nReTpW1OqhYKVjMS291JIZfnzc130_assertion description "[These findings expand the number of APP mutations linked to hereditary cerebral hemorrhage with amyloidosis, reinforcing the link between this phenotype and codon 693 of APP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183435.RAuqLxfW3v8ZLySRRc_nReTpW1OqhYKVjMS291JIZfnzc130_provenance.