Matches in Nanopublications for { ?s ?p "[Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- assertion description "[Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_assertion description "[Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.
- NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_assertion description "[Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_provenance.
- NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_assertion description "[Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.
- NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_assertion description "[Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_provenance.