Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance.
- NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_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." NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance.
- NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_assertion evidence source_evidence_literature NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance.
- NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_assertion SIO_000772 15869605 NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance.
- NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_assertion wasDerivedFrom befree-20150227 NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance.
- NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_assertion wasGeneratedBy ECO_0000203 NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP776331.RA0h3XHkts0Jt6Ieh-whLLaw7qSxXMbmFu7heUigGFFXQ130_provenance.