Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion> ?p ?o ?g. }
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- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion type Assertion NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_head.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion wasGeneratedBy ECO_0000203 NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion wasDerivedFrom befree-2016 NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion SIO_000772 18853458 NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion evidence source_evidence_literature NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion description "[Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.