Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_assertion> ?p ?o ?g. }
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- NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_assertion type Assertion NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_head.
- 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.
- NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_assertion evidence source_evidence_literature NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_provenance.
- NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_assertion SIO_000772 22503161 NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_provenance.
- NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_assertion wasDerivedFrom befree-20150227 NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_provenance.
- NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_assertion wasGeneratedBy ECO_0000203 NP247036.RA2h3pRwhJAW9WvUb-rzbMPkvnMctMXh_4VT_SyS3m6bg130_provenance.