Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance.
- NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_assertion description "[Over 70 transthyretin (TTR) mutations have been associated with hereditary amyloidoses, which are all autosomal dominant disorders with adult age of onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance.
- NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_assertion evidence source_evidence_literature NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance.
- NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_assertion SIO_000772 11412857 NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance.
- NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_assertion wasDerivedFrom befree-2016 NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance.
- NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_assertion wasGeneratedBy ECO_0000203 NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance.
- befree-2016 importedOn "2016-02-19" NP321343.RAR6humFN3Hz_-fO_dFQgeR2FC7AZJRzcjzsCPeDV7VXM130_provenance.