Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance.
- NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_assertion description "[A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer's disease and spastic paraparesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance.
- NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_assertion evidence source_evidence_literature NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance.
- NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_assertion SIO_000772 18637955 NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance.
- NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_assertion wasDerivedFrom befree-20150227 NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance.
- NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_assertion wasGeneratedBy ECO_0000203 NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP650670.RABKgfu_aQMAzlm3_b55gLgQqR-Bjao6mjKfa0aS4p2GM130_provenance.