Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance.
- NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_assertion description "[It is most frequently seen in patients with hereditary transthyretin (TTR) amyloidosis, but is also present in 20% of patients with systemic immunoglobulin light chain (primary) amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance.
- NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_assertion evidence source_evidence_literature NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance.
- NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_assertion SIO_000772 17554795 NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance.
- NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_assertion wasDerivedFrom befree-20140225 NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance.
- NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_assertion wasGeneratedBy ECO_0000203 NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP440937.RAMBe_6IPLsY4LPwWsT0VJitu8tJPIoW-ZMBqqhfygvv0130_provenance.