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- NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_assertion type Assertion NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_head.
- NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_assertion wasGeneratedBy ECO_0000203 NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_provenance.
- NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_assertion wasDerivedFrom befree-20150227 NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_provenance.
- NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_assertion SIO_000772 12134148 NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_provenance.
- NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_assertion evidence source_evidence_literature NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_provenance.
- NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_assertion description "[SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868257.RA-ABkS5IQ4OAgiAXtecrFofrOnNw1XayqMhedUkyl9ak130_provenance.