Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_assertion> ?p ?o ?g. }
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- NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_assertion type Assertion NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_head.
- NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_assertion description "[These results suggest that the frequency of SPAST mutations is higher among Japanese patients with autosomal dominant Hereditary spastic paraplegia (HSP), although SPAST mutations are also observed in patients with sporadic spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_provenance.
- NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_assertion evidence source_evidence_literature NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_provenance.
- NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_assertion SIO_000772 16788734 NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_provenance.
- NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_assertion wasDerivedFrom lhgdn-20090331 NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_provenance.
- NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_assertion wasGeneratedBy ECO_0000203 NP217937.RA4RfOX5J9cvaTVt3X2Yf9HM9d5Uij--qhvhLNR5eFF8Q130_provenance.