Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_assertion> ?p ?o ?g. }
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- NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_assertion type Assertion NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_head.
- NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_assertion wasGeneratedBy ECO_0000203 NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_provenance.
- NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_assertion wasDerivedFrom befree-20140225 NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_provenance.
- NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_assertion SIO_000772 17094098 NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_provenance.
- NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_assertion evidence source_evidence_literature NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_provenance.
- NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_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." NP418192.RAiXMlh16U1ozqiU7owRANLXPjAAK9z0pCK5TPTdUgfv0130_provenance.