Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_assertion type Assertion NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_head.
- NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_assertion description "[Autosomal dominant familial spastic paraplegia (FSP) is a genetically heterogeneous neurodegenerative disorder displaying anticipation for which three loci have been mapped to the chromosomal positions 14q11.2-q24.3 (SPG3), 2p21-p24 (SPG4) and 15q11.1 (SPG6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_provenance.
- NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_assertion evidence source_evidence_literature NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_provenance.
- NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_assertion SIO_000772 9736780 NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_provenance.
- NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_assertion wasDerivedFrom befree-20140225 NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_provenance.
- NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_assertion wasGeneratedBy ECO_0000203 NP490125.RAjPG56eyIP1MfKJDfmZXxjJ5BBLRS8-l-RxE76GfDNnc130_provenance.