Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.
- NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_assertion description "[Discovery of this new mutation confirms the association between fibrinogen A alpha chain variant and hereditary renal amyloidosis and establishes a new biochemical subtype of amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.
- NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_assertion evidence source_evidence_literature NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.
- NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_assertion SIO_000772 8113408 NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.
- NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_assertion wasDerivedFrom befree-20140225 NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.
- NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_assertion wasGeneratedBy ECO_0000203 NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.
- befree-20140225 importedOn "2014-02-25" NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.