Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_assertion type Assertion NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_head.
- NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_assertion wasGeneratedBy ECO_0000203 NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_provenance.
- NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_assertion wasDerivedFrom befree-2016 NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_provenance.
- NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_assertion SIO_000772 18580586 NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_provenance.
- NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_assertion evidence source_evidence_literature NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_provenance.
- NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_assertion description "[The objective is to describe clinical and neuropathologic features of a family with a PSEN1 mutation that has been reported previously, without autopsy confirmation, in a single Greek family whose affected members presented with memory loss in their 30s, as well as variable limb spasticity and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678797.RAhKCT5L-jdopiR8m2hE82xQnHXJdjMBOsLVQUtAxQIE4130_provenance.