Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance.
- NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_assertion description "[The presence of an inherited thrombophilia should not alter the intensity of anticoagulant therapy, given that antithrombin, protein C, or protein S deficiency, factor V Leiden, and the prothrombin G20210A mutation are not unusually anticoagulant resistant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance.
- NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_assertion evidence source_evidence_literature NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance.
- NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_assertion SIO_000772 15706484 NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance.
- NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_assertion wasDerivedFrom befree-2016 NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance.
- NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_assertion wasGeneratedBy ECO_0000203 NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance.
- befree-2016 importedOn "2016-02-19" NP480654.RAX2Sw6CJ_IZKacvE5LezHQNaTQnUZYNoMbCzcFtZCmLc130_provenance.