Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_assertion type Assertion NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_head.
- NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_assertion description "[Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_provenance.
- NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_assertion evidence source_evidence_curated NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_provenance.
- NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_assertion SIO_000772 15009458 NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_provenance.
- NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_assertion wasDerivedFrom uniprot-20130724 NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_provenance.
- NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_assertion wasGeneratedBy ECO_0000218 NP196.RAX8SVsbe5uI8U57yDxRQtRRzG1nxOU6yxqF9rBj4NG8I130_provenance.