Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.
- NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_assertion description "[the mutation in prothrombin that may have a role in hereditary prothrombin deficiency in Indian patients is named'Prothrombin Vellore 1'and is an Ala362Thr mutation]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.
- NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_assertion evidence source_evidence_literature NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.
- NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_assertion SIO_000772 15892853 NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.
- NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_assertion wasDerivedFrom lhgdn-20090331 NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.
- NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_assertion wasGeneratedBy ECO_0000203 NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP211790.RAMuVtjmkhgaVGxUBBExPLo_iI4X0RPg8tNsEJxwT18K0130_provenance.