Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.