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- source_evidence_literature type ECO_0000212 NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.
- NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.
- NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_assertion evidence source_evidence_literature NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.
- NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_assertion SIO_000772 23797140 NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.
- NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_assertion wasDerivedFrom befree-20140225 NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.
- NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_assertion wasGeneratedBy ECO_0000203 NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP561675.RAoC9_2Dt16G7gROazVUaA3X27ySg_xVub_e5mB4beJ-U130_provenance.