Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion> ?p ?o ?g. }
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- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion type Assertion NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_head.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion description "[Partial SPAST deletions represent an underestimated cause of autosomal dominant hereditary spastic paraplegia/SPAST deletions are likely to act via haploinsufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion evidence source_evidence_literature NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion SIO_000772 17035675 NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion wasDerivedFrom lhgdn-20090331 NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion wasGeneratedBy ECO_0000203 NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.