Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_assertion> ?p ?o ?g. }
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- NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_assertion type Assertion NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_head.
- NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.
- NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_assertion evidence source_evidence_literature NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.
- NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_assertion SIO_000772 10480368 NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.
- NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_assertion wasDerivedFrom befree-20150227 NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.
- NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_assertion wasGeneratedBy ECO_0000203 NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.