Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_assertion> ?p ?o ?g. }
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- NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_assertion type Assertion NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_head.
- NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_assertion wasGeneratedBy ECO_0000203 NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_provenance.
- NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_assertion wasDerivedFrom befree-20150227 NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_provenance.
- NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_assertion SIO_000772 17094098 NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_provenance.
- NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_assertion evidence source_evidence_literature NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_provenance.
- NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_assertion description "[Transthyretin amyloid neuropathy of type 1 (Swedish-Portuguese type) is an autosomally inherited progressive disease with a Val30Met mutation, causing generalized sensory-motor polyneuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761817.RAAJtWu8qsvWWD1goBpX20DHkstjRALzpNspHtMEXfPY4130_provenance.