Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_assertion> ?p ?o ?g. }
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- NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_assertion type Assertion NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_head.
- NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_assertion description "[Functional deficiency or absence of the human von Willebrand factor (VWF)-cleaving protease (VWF-cp), recently termed ADAMTS13, has been shown to cause acquired and congenital thrombotic thrombocytopenic purpura (TTP), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_provenance.
- NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_assertion evidence source_evidence_literature NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_provenance.
- NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_assertion SIO_000772 15869605 NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_provenance.
- NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_assertion wasDerivedFrom befree-20140225 NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_provenance.
- NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_assertion wasGeneratedBy ECO_0000203 NP657667.RACcGzO-nRVCD04PO7XmqNpUfpcdXisX7S6IPUWl6WE7E130_provenance.