Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_assertion> ?p ?o ?g. }
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- NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_assertion type Assertion NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_head.
- NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_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." NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_provenance.
- NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_assertion evidence source_evidence_literature NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_provenance.
- NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_assertion SIO_000772 9736780 NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_provenance.
- NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_assertion wasDerivedFrom befree-20140225 NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_provenance.
- NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_assertion wasGeneratedBy ECO_0000203 NP715815.RAA3eVXCYW3-zLGFy9w07YcY2ZDqfIhp6WJo5hvIsdtSI130_provenance.