Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_assertion> ?p ?o ?g. }
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- NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_assertion type Assertion NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_head.
- NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_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." NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_provenance.
- NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_assertion evidence source_evidence_literature NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_provenance.
- NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_assertion SIO_000772 9736780 NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_provenance.
- NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_assertion wasDerivedFrom befree-2016 NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_provenance.
- NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_assertion wasGeneratedBy ECO_0000203 NP1403915.RA7ytUwBuDsihIQVOP2CC4UoFP1wstunldGu4lbHxpoxg130_provenance.