Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance.
- NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_assertion description "[Although the assay is thought to accurately measure protein C activity in patients taking warfarin, one cannot evaluate such patients for hereditary functional protein C deficiency because treatment with warfarin will itself reduce the ratio of protein C activity to antigen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance.
- NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_assertion evidence source_evidence_literature NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance.
- NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_assertion SIO_000772 3826014 NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance.
- NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_assertion wasDerivedFrom befree-2016 NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance.
- NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_assertion wasGeneratedBy ECO_0000203 NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1303682.RAop0sYehgSZ7EeJ1soxc1MRl3oH6gLn4cDcMeqYK-CTU130_provenance.