Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP204764.RAZLByf2WXU5ZAWXWS4v5nXcEDxYV1HvaObLF00_mQiz4130_provenance.