Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_assertion> ?p ?o ?g. }
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- NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_assertion type Assertion NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_head.
- NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_assertion description "[Thus, a prealbumin variant and its fragments constitute the amyloid fibrils in a heredofamilial amyloidosis syndrome of dominant inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_provenance.
- NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_assertion evidence source_evidence_literature NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_provenance.
- NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_assertion SIO_000772 6300852 NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_provenance.
- NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_assertion wasDerivedFrom befree-2016 NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_provenance.
- NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_assertion wasGeneratedBy ECO_0000203 NP1305469.RAptTuoSg7dyX01I-qVg0E3TtKL_CPzV3g8TxzBpQhXgU130_provenance.