Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_assertion> ?p ?o ?g. }
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- NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_assertion type Assertion NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_head.
- 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.
- NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_assertion evidence source_evidence_literature NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_provenance.
- NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_assertion SIO_000772 22503161 NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_provenance.
- NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_assertion wasDerivedFrom befree-2016 NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_provenance.
- NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_assertion wasGeneratedBy ECO_0000203 NP974762.RAWlk8l2b9_edPzV0ZBQxoBDS67RSXpNbRy237iuhSgw0130_provenance.