Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.
- NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_assertion description "[We conclude that this kindred demonstrates a considerable overlap between cerebellar ataxia and spastic paraplegia, emphasizing the marked clinical heterogeneity of HSP associated with spastin mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.
- NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_assertion evidence source_evidence_literature NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.
- NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_assertion SIO_000772 15667412 NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.
- NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_assertion wasDerivedFrom befree-20140225 NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.
- NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_assertion wasGeneratedBy ECO_0000203 NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.