Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion> ?p ?o ?g. }
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- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion type Assertion NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_head.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion description "[Loss of function of paraplegin (encoded by the SPG7 gene) causes hereditary spastic paraplegia, a disease characterized by retrograde degeneration of cortical motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion evidence source_evidence_literature NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion SIO_000772 19289403 NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion wasDerivedFrom befree-20140225 NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.
- NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_assertion wasGeneratedBy ECO_0000203 NP316894.RAYDYYMlL9EnkHFuIYfPSUqUQ-dssBDFWfRX6fKTDwF08130_provenance.