Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_assertion> ?p ?o ?g. }
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- NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_assertion type Assertion NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_head.
- NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_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." NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_provenance.
- NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_assertion evidence source_evidence_literature NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_provenance.
- NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_assertion SIO_000772 9736780 NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_provenance.
- NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_assertion wasDerivedFrom befree-20150227 NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_provenance.
- NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_assertion wasGeneratedBy ECO_0000203 NP900899.RA0MF4Ys5_SqvgnOOUeLl5-XarhNUcpsldQk58XmYQ-xg130_provenance.