Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_assertion type Assertion NP722569.RA2Msq2XqlNQ2DueiQMoHWkT-mVLD9w6yC7lQiBF5L4zk130_head.
- 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.