Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance.
- NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_assertion description "[We prospectively included 20 patients (12 male and eight female patients, mean age 47.9 years, range 26-66) with confirmed mutation in the transthyretin gene: 13 with symptomatic polyneuropathy and seven asymptomatic gene carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance.
- NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_assertion evidence source_evidence_literature NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance.
- NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_assertion SIO_000772 25526974 NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance.
- NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_assertion wasDerivedFrom befree-2016 NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance.
- NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_assertion wasGeneratedBy ECO_0000203 NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249834.RAHzIdXZf6U3-fmu-OJdYvEIsvRDBLInnPvWIim--GThc130_provenance.