Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_assertion> ?p ?o ?g. }
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- NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_assertion type Assertion NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_head.
- NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_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." NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance.
- NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_assertion evidence source_evidence_literature NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance.
- NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_assertion SIO_000772 17035675 NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance.
- NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_assertion wasDerivedFrom lhgdn-20090331 NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance.
- NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_assertion wasGeneratedBy ECO_0000203 NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance.