Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion> ?p ?o ?g. }
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- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion type Assertion NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_head.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion description "[Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant hereditary SPG caused by mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion evidence source_evidence_literature NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion SIO_000772 20857310 NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion wasDerivedFrom befree-20140225 NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.
- NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_assertion wasGeneratedBy ECO_0000203 NP426399.RA-d87ezaLXN_Mc7nib7iAZoIT1wTmg6PEmoS6ZyFvFR4130_provenance.