Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.
- NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_assertion description "[The Portuguese type of familial amyloid polyneuropathy (FAP type I), a disabling autosomal dominant disorder with onset in early adult life, is caused by a point mutation in the transthyretin (TTR; previously known as prealbumin) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.
- NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_assertion evidence source_evidence_literature NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.
- NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_assertion SIO_000772 2564060 NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.
- NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_assertion wasDerivedFrom befree-20140225 NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.
- NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_assertion wasGeneratedBy ECO_0000203 NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_provenance.