Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_assertion> ?p ?o ?g. }
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- NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_assertion type Assertion NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_head.
- NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_assertion description "[Mutations in the SPG7 gene encoding a mitochondrial protein termed paraplegin, are responsible for a recessive form of hereditary spastic paraparesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_provenance.
- NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_assertion evidence source_evidence_literature NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_provenance.
- NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_assertion SIO_000772 18200586 NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_provenance.
- NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_assertion wasDerivedFrom befree-20140225 NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_provenance.
- NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_assertion wasGeneratedBy ECO_0000203 NP693565.RANc-yNUV7HPMZ-74kMfd9h4WmwR-kzGX5HUMePKQWNG0130_provenance.