Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance.
- NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_assertion description "[SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance.
- NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_assertion evidence source_evidence_literature NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance.
- NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_assertion SIO_000772 19194956 NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance.
- NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_assertion wasDerivedFrom befree-20150227 NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance.
- NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_assertion wasGeneratedBy ECO_0000203 NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance.
- befree-20150227 importedOn "2015-02-27" NP948448.RAmFpV5kw_0vqUZymArHlvM7wEFldHu0FRJhJyLKqT9Ts130_provenance.