Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_assertion> ?p ?o ?g. }
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- NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_assertion type Assertion NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_head.
- NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_assertion wasGeneratedBy ECO_0000203 NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_provenance.
- NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_assertion wasDerivedFrom befree-20140225 NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_provenance.
- NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_assertion SIO_000772 16423463 NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_provenance.
- NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_assertion evidence source_evidence_literature NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_provenance.
- NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_assertion description "[Furthermore, we found an intronic +17G>C polymorphism in PEN2 which, in homozygous form, was greater in early onset Alzheimer's disease (EOAD) compared to controls, and one haplotype in the NCSTN gene which was linked to EOAD and familial AD (FAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266524.RAbTmhyQgYN5FIBrnRPWgJLkcpEeNLHwgKEb3kPXXn2hI130_provenance.