Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance.
- NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_assertion description "[Genomic DNA from patients with HVOTO and healthy controls was analyzed for the presence of FVL and prothrombin gene G20210A mutations, using PCR and restriction-fragment length polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance.
- NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_assertion evidence source_evidence_literature NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance.
- NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_assertion SIO_000772 16361766 NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance.
- NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_assertion wasDerivedFrom befree-2016 NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance.
- NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_assertion wasGeneratedBy ECO_0000203 NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance.
- befree-2016 importedOn "2016-02-19" NP527517.RARxKvnrVaL0VoBQdNhCfGy72ctDGMHdHRT1kO3Xf2ntM130_provenance.