Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_assertion> ?p ?o ?g. }
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- NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_assertion type Assertion NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_head.
- NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_assertion description "[As this is a third independent case of protein C Tochigi with thromboembolism, the mutation of Arg169 (CGG) to Trp169 (TGG) in the protein C gene may be a `hot spot` and a common type of genetic lesion in congenital protein C deficiency with thromboembolic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_provenance.
- NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_assertion evidence source_evidence_literature NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_provenance.
- NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_assertion SIO_000772 1596024 NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_provenance.
- NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_assertion wasDerivedFrom befree-20140225 NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_provenance.
- NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_assertion wasGeneratedBy ECO_0000203 NP264568.RAsBk6Hf08mnavkCWUK1WqZdKZNphJOGtqdTo1YtKNBfw130_provenance.