Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.
- NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.
- NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_assertion evidence source_evidence_literature NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.
- NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_assertion SIO_000772 24569455 NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.
- NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_assertion wasDerivedFrom befree-2016 NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.
- NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_assertion wasGeneratedBy ECO_0000203 NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1158090.RAsvcP8IJSdjrkufxYj_G8Bxns56poe7-huDp_NJ6B8Vk130_provenance.